esv3833118

Organism: Homo sapiens

Study:estd219 (1000 Genomes Consortium Phase 3 Integrated SV)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:61
Validation:Not tested
Clinical Assertions: No
Region Size:9,974

Publication(s):1000 Genomes Consortium Phase 3 Integrated SV

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 172 SVs from 48 studies. See in: genome view

Remapped(Score: Perfect):173,489,598-173,500,571

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3833118	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
esv3833118	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv18599981	deletion	HG01075	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,747
essv18599982	deletion	HG01164	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,147
essv18599983	deletion	HG01989	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,773
essv18599984	deletion	HG02111	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,795
essv18599985	deletion	HG02330	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,018
essv18599986	deletion	HG02477	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,766
essv18599987	deletion	HG02570	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,147
essv18599988	deletion	HG02621	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,967
essv18599989	deletion	HG02675	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,193
essv18599990	deletion	HG02676	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,958
essv18599991	deletion	HG02722	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,008
essv18599992	deletion	HG02760	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,040
essv18599993	deletion	HG02798	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,098
essv18599994	deletion	HG02817	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,626
essv18599995	deletion	HG02854	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,874
essv18599996	deletion	HG02938	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,461
essv18599997	deletion	HG02971	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,790
essv18599998	deletion	HG03025	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,706
essv18599999	deletion	HG03046	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,832
essv18600000	deletion	HG03066	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,908
essv18600001	deletion	HG03069	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,750
essv18600002	deletion	HG03079	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,021
essv18600003	deletion	HG03084	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,128
essv18600004	deletion	HG03091	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,965
essv18600005	deletion	HG03105	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,062
essv18600006	deletion	HG03108	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,906
essv18600007	deletion	HG03117	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Homozygous	3,895
essv18600008	deletion	HG03124	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,169
essv18600009	deletion	HG03139	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,152
essv18600010	deletion	HG03247	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,573
essv18600011	deletion	HG03370	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,015
essv18600012	deletion	HG03376	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,901
essv18600013	deletion	HG03378	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,840
essv18600014	deletion	HG03380	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,578
essv18600015	deletion	HG03394	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,416
essv18600016	deletion	HG03451	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,085
essv18600017	deletion	HG03460	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,875
essv18600018	deletion	HG03469	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,901
essv18600019	deletion	HG03472	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,159
essv18600020	deletion	HG03511	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,980
essv18600021	deletion	NA18488	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,792
essv18600022	deletion	NA18504	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,958
essv18600023	deletion	NA18871	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,552
essv18600024	deletion	NA18910	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,161
essv18600025	deletion	NA19038	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,670
essv18600026	deletion	NA19098	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,311
essv18600027	deletion	NA19116	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,717
essv18600028	deletion	NA19130	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,165
essv18600029	deletion	NA19184	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,210
essv18600030	deletion	NA19257	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,064
essv18600031	deletion	NA19312	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,772
essv18600032	deletion	NA19319	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,273
essv18600033	deletion	NA19331	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,440
essv18600034	deletion	NA19374	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,853
essv18600035	deletion	NA19399	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,792
essv18600036	deletion	NA19466	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,912
essv18600037	deletion	NA19704	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,768
essv18600038	deletion	NA19711	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,886
essv18600039	deletion	NA20126	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,500
essv18600040	deletion	NA20359	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,821
essv18600041	deletion	NA20362	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,175

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv18599981	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599982	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599983	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599984	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599985	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599986	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599987	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599988	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599989	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599990	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599991	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599992	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599993	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599994	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599995	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599996	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599997	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599998	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599999	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600000	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600001	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600002	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600003	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600004	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600005	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600006	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600007	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600008	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600009	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600010	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600011	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600012	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600013	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600014	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600015	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600016	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600017	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600018	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600019	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600020	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600021	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600022	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600023	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600024	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600025	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600026	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600027	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600028	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600029	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600030	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600031	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600032	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600033	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600034	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600035	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600036	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600037	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600038	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600039	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600040	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18600041	Remapped	Perfect	NC_000003.12:g.(17 3489598_173490098) _(173500071_173500 571)del	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,490,098 (-500, +0)	173,500,071 (-0, +500)
essv18599981	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599982	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599983	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599984	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599985	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599986	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599987	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599988	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599989	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599990	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599991	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599992	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599993	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599994	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599995	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599996	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599997	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599998	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18599999	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600000	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600001	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600002	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600003	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600004	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600005	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600006	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600007	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600008	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600009	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600010	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600011	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600012	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600013	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600014	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600015	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600016	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600017	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600018	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)
essv18600019	Submitted genomic		NC_000003.11:g.(17 3207388_173207888) _(173217861_173218 361)del	GRCh37 (hg19)		NC_000003.11	Chr3	173,207,888 (-500, +0)	173,217,861 (-0, +500)

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dbVar

Database of genomic structural variation

esv3833118

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.