esv3831107

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:45
Validation:Not tested
Clinical Assertions: No
Region Size:14,519

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: 154 SVs from 45 studies. See in: genome view

Remapped(Score: Perfect):87,838,823-87,855,341

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3831107	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
esv3831107	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv18375811	deletion	HG01914	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,133
essv18375812	deletion	HG01915	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,764
essv18375813	deletion	HG01958	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,843
essv18375814	deletion	HG02010	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,026
essv18375815	deletion	HG02054	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,702
essv18375816	deletion	HG02256	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,624
essv18375817	deletion	HG02284	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,143
essv18375818	deletion	HG02461	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,157
essv18375819	deletion	HG02505	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,066
essv18375820	deletion	HG02545	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,951
essv18375821	deletion	HG02582	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,147
essv18375822	deletion	HG02583	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,904
essv18375823	deletion	HG02611	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Homozygous	4,051
essv18375824	deletion	HG02757	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,898
essv18375825	deletion	HG02896	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,590
essv18375826	deletion	HG03039	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,126
essv18375827	deletion	HG03040	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,875
essv18375828	deletion	HG03077	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,244
essv18375829	deletion	HG03079	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,021
essv18375830	deletion	HG03082	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,942
essv18375831	deletion	HG03124	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,169
essv18375832	deletion	HG03159	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,802
essv18375833	deletion	HG03160	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,844
essv18375834	deletion	HG03224	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,231
essv18375835	deletion	HG03267	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,658
essv18375836	deletion	HG03313	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,432
essv18375837	deletion	HG03366	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,505
essv18375838	deletion	HG03388	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,983
essv18375839	deletion	HG03410	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,732
essv18375840	deletion	HG03538	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,894
essv18375841	deletion	HG03624	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,891
essv18375842	deletion	NA18501	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,193
essv18375843	deletion	NA18508	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,090
essv18375844	deletion	NA18874	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,245
essv18375845	deletion	NA18907	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,088
essv18375846	deletion	NA19024	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,895
essv18375847	deletion	NA19031	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,722
essv18375848	deletion	NA19121	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,028
essv18375849	deletion	NA19144	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,589
essv18375850	deletion	NA19197	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,084
essv18375851	deletion	NA19256	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,295
essv18375852	deletion	NA19384	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,966
essv18375853	deletion	NA19385	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,057
essv18375854	deletion	NA19440	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,830
essv18375855	deletion	NA19984	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,753

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv18375811	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375812	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375813	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375814	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375815	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375816	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375817	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375818	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375819	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375820	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375821	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375822	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375823	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375824	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375825	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375826	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375827	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375828	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375829	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375830	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375831	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375832	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375833	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375834	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375835	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375836	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375837	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375838	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375839	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375840	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375841	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375842	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375843	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375844	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375845	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375846	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375847	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375848	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375849	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375850	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375851	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375852	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375853	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375854	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375855	Remapped	Perfect	NC_000003.12:g.(87 838823_87840323)_( 87853841_87855341) del	GRCh38.p12	First Pass	NC_000003.12	Chr3	87,839,823 (-1000, +500)	87,854,341 (-500, +1000)
essv18375811	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375812	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375813	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375814	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375815	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375816	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375817	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375818	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375819	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375820	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375821	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375822	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375823	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375824	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375825	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375826	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375827	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375828	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375829	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375830	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375831	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375832	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375833	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375834	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375835	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375836	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375837	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375838	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375839	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375840	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375841	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375842	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375843	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375844	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375845	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375846	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375847	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375848	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375849	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375850	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375851	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375852	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375853	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375854	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)
essv18375855	Submitted genomic		NC_000003.11:g.(87 887973_87889473)_( 87902991_87904491) del	GRCh37 (hg19)		NC_000003.11	Chr3	87,888,973 (-1000, +500)	87,903,491 (-500, +1000)

dbVar

Database of genomic structural variation

esv3831107

Links to Other Resources

Genome View

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.