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dbVar

Database of genomic structural variation

nsv6631410

Organism: Homo sapiens

Study:nstd224 (Zarrei et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:7
Validation:Not tested
Clinical Assertions: No
Region Size:10,222

Publication(s):Zarrei et al. 2023

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: 336 SVs from 63 studies. See in: genome view

Remapped(Score: Perfect):35,787,045-35,797,266

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6631410	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	35,787,045	35,797,266
nsv6631410	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	35,754,822	35,765,043

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18281979	duplication	OSC0213	SNP array	Probe signal intensity	nssv18282592, nssv18282296
nssv18283599	duplication	OSC2336	SNP array	Probe signal intensity	nssv18283258, nssv18283259, nssv18283600
nssv18287061	duplication	OSC3097	SNP array	Probe signal intensity	11
nssv18292793	duplication	OSC4041	SNP array	Probe signal intensity	7
nssv18297602	duplication	OSC4881	SNP array	Probe signal intensity	6
nssv18312733	duplication	OSC0789	SNP array	Probe signal intensity	6
nssv18323637	duplication	OSC1653	SNP array	Probe signal intensity	7

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18281979	Remapped	Perfect	NC_000006.12:g.(?_ 35787045)_(3579726 6_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	35,787,045	35,797,266
nssv18283599	Remapped	Perfect	NC_000006.12:g.(?_ 35787045)_(3579726 6_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	35,787,045	35,797,266
nssv18287061	Remapped	Perfect	NC_000006.12:g.(?_ 35787045)_(3579726 6_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	35,787,045	35,797,266
nssv18292793	Remapped	Perfect	NC_000006.12:g.(?_ 35787045)_(3579726 6_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	35,787,045	35,797,266
nssv18297602	Remapped	Perfect	NC_000006.12:g.(?_ 35787045)_(3579726 6_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	35,787,045	35,797,266
nssv18312733	Remapped	Perfect	NC_000006.12:g.(?_ 35787045)_(3579726 6_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	35,787,045	35,797,266
nssv18323637	Remapped	Perfect	NC_000006.12:g.(?_ 35787045)_(3579726 6_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	35,787,045	35,797,266
nssv18281979	Submitted genomic		NC_000006.11:g.(?_ 35754822)_(3576504 3_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	35,754,822	35,765,043
nssv18283599	Submitted genomic		NC_000006.11:g.(?_ 35754822)_(3576504 3_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	35,754,822	35,765,043
nssv18287061	Submitted genomic		NC_000006.11:g.(?_ 35754822)_(3576504 3_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	35,754,822	35,765,043
nssv18292793	Submitted genomic		NC_000006.11:g.(?_ 35754822)_(3576504 3_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	35,754,822	35,765,043
nssv18297602	Submitted genomic		NC_000006.11:g.(?_ 35754822)_(3576504 3_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	35,754,822	35,765,043
nssv18312733	Submitted genomic		NC_000006.11:g.(?_ 35754822)_(3576504 3_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	35,754,822	35,765,043
nssv18323637	Submitted genomic		NC_000006.11:g.(?_ 35754822)_(3576504 3_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	35,754,822	35,765,043

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

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