nsv4377863

Organism: Homo sapiens

Study:nstd173 (Zarrei et al. 2019)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:57
Validation:Not tested
Clinical Assertions: No
Region Size:25,603

Publication(s):Zarrei et al. 2019

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: 541 SVs from 77 studies. See in: genome view

Remapped(Score: Perfect):51,628,547-51,654,149

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4377863	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nsv4377863	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	52,131,800	52,157,402

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15611681	copy number loss	1-0653-002	SNP array	Genotyping	28
nssv15612794	copy number loss	1-0653-004	SNP array	Genotyping	27
nssv15613062	copy number loss	1-0662-004	SNP array	Genotyping	21
nssv15613495	copy number loss	1-0685-003	SNP array	Genotyping	20
nssv15614286	copy number loss	1-0718-003	SNP array	Genotyping	35
nssv15615025	copy number loss	1-0737-003	SNP array	Genotyping	16
nssv15615405	copy number loss	1-0771-003	SNP array	Genotyping	20
nssv15615648	copy number loss	1-0760-003	SNP array	Genotyping	22
nssv15616929	copy number loss	1-0826-003	SNP array	Genotyping	27
nssv15617286	copy number loss	1-0832-003	SNP array	Genotyping	21
nssv15617463	copy number loss	1-0845-003	SNP array	Genotyping	36
nssv15618110	copy number loss	1-0884-003	SNP array	Genotyping	33
nssv15620810	copy number loss	1-0958-003	SNP array	Genotyping	22
nssv15623661	copy number loss	1-0271-002	SNP array	Genotyping	37
nssv15624100	copy number loss	1-0291-002	SNP array	Genotyping	30
nssv15625935	copy number loss	1-0432-005	SNP array	Genotyping	21
nssv15626019	copy number loss	1-0405-003	SNP array	Genotyping	16
nssv15626277	copy number loss	1-0442-001	SNP array	Genotyping	18
nssv15626899	copy number loss	1-0456-004	SNP array	Genotyping	23
nssv15628282	copy number loss	1-0509-003	SNP array	Genotyping	16
nssv15628855	copy number loss	1-0559-002	SNP array	Genotyping	20
nssv15629270	copy number loss	1-0576-001	SNP array	Genotyping	19
nssv15629478	copy number loss	1-0560-003	SNP array	Genotyping	21
nssv15629787	copy number loss	1-0578-003	SNP array	Genotyping	24
nssv15630204	copy number loss	1-0555-002	SNP array	Genotyping	27
nssv15630650	copy number loss	1-0600-003	SNP array	Genotyping	25
nssv15630732	copy number loss	1-0619-003	SNP array	Genotyping	25
nssv15631550	copy number loss	1-0638-001	SNP array	Genotyping	12
nssv15632767	copy number loss	10-0008-001	SNP array	Genotyping	27
nssv15633251	copy number loss	11-0016-003	SNP array	Genotyping	23
nssv15635255	copy number loss	12-4139-003	SNP array	Genotyping	27
nssv15640919	copy number loss	14-0318-003	SNP array	Genotyping	19
nssv15642184	copy number loss	16-1002-001	SNP array	Genotyping	20
nssv15645014	copy number loss	2-0272-002	SNP array	Genotyping	19
nssv15654705	copy number loss	3-0193-000	SNP array	Genotyping	19
nssv15657346	copy number loss	3-0380-002	SNP array	Genotyping	28
nssv15659717	copy number loss	4-0070-003	SNP array	Genotyping	24
nssv15659768	copy number loss	4-0073-001	SNP array	Genotyping	22
nssv15659815	copy number loss	4-0073-003	SNP array	Genotyping	21
nssv15665635	copy number loss	7-0082-003	SNP array	Genotyping	15
nssv15668267	copy number loss	7-0187-003	SNP array	Genotyping	31
nssv15670558	copy number loss	7-0193-003	SNP array	Genotyping	16
nssv15670809	copy number loss	7-0295-003	SNP array	Genotyping	24
nssv15673186	copy number loss	9-0029-002	SNP array	Genotyping	19
nssv15673419	copy number loss	9-0030-002	SNP array	Genotyping	24
nssv15673518	copy number loss	9-0034-002	SNP array	Genotyping	27
nssv15676928	copy number loss	188699	SNP array	Genotyping	23
nssv15679458	copy number loss	227244	SNP array	Genotyping	29
nssv15679756	copy number loss	207275	SNP array	Genotyping	20
nssv15680815	copy number loss	230094S	SNP array	Genotyping	18
nssv15686640	copy number loss	OCD152-SM-1338(188608)	SNP array	Genotyping	21
nssv15695669	copy number loss	OCD92-JW-1312	SNP array	Genotyping	14
nssv15696545	copy number gain	160592	SNP array	Genotyping	21
nssv15697556	copy number loss	240711	SNP array	Genotyping	27
nssv15700450	copy number loss	226749	SNP array	Genotyping	22
nssv15701398	copy number loss	79240	SNP array	Genotyping	12
nssv15701596	copy number loss	224728	SNP array	Genotyping	26

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15611681	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15612794	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15613062	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15613495	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15614286	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15615025	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15615405	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15615648	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15616929	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15617286	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15617463	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15618110	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15620810	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15623661	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15624100	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15625935	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15626019	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15626277	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15626899	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15628282	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15628855	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15629270	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15629478	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15629787	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15630204	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15630650	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15630732	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15631550	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15632767	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15633251	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15635255	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15640919	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15642184	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15645014	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15654705	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15657346	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15659717	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15659768	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15659815	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15665635	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15668267	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15670558	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15670809	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15673186	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15673419	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15673518	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15676928	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15679458	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15679756	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15680815	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15686640	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15695669	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15696545	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)dup	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15697556	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15700450	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15701398	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15701596	Remapped	Perfect	NC_000019.10:g.(?_ 51628547)_(5165414 9_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	51,628,547	51,654,149
nssv15611681	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15612794	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15613062	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15613495	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15614286	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15615025	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15615405	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15615648	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15616929	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15617286	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15617463	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15618110	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15620810	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15623661	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15624100	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15625935	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15626019	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15626277	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15626899	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15628282	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15628855	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15629270	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15629478	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15629787	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15630204	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15630650	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15630732	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15631550	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15632767	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15633251	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15635255	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15640919	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15642184	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15645014	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15654705	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15657346	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15659717	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15659768	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15659815	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15665635	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15668267	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15670558	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402
nssv15670809	Submitted genomic		NC_000019.9:g.(?_5 2131800)_(52157402 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	52,131,800	52,157,402

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dbVar

Database of genomic structural variation

nsv4377863

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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

No genotype data were submitted for this variant