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dbVar

Database of genomic structural variation

nsv818491

Organism: Homo sapiens

Study:nstd64 (Wang et al. 2007)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:NCBI35 (hg17)

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:134,679

Publication(s):Wang et al. 2007

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

Remapped(Score: Perfect):19,373,648-19,508,326

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv818491	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	19,373,648	19,508,326
nsv818491	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	19,413,271	19,547,949
nsv818491	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000007.11	Chr7	19,186,511	19,321,189

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv1418002	copy number gain	NA07345	SNP array	Probe signal intensity	19
nssv1418003	copy number gain	NA07348	SNP array	Probe signal intensity	21

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv1418002	Remapped	Perfect	NC_000007.14:g.(?_ 19373648)_(1950832 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	19,373,648	19,508,326
nssv1418003	Remapped	Perfect	NC_000007.14:g.(?_ 19373648)_(1950832 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	19,373,648	19,508,326
nssv1418002	Remapped	Perfect	NC_000007.13:g.(?_ 19413271)_(1954794 9_?)dup	GRCh37.p13	First Pass	NC_000007.13	Chr7	19,413,271	19,547,949
nssv1418003	Remapped	Perfect	NC_000007.13:g.(?_ 19413271)_(1954794 9_?)dup	GRCh37.p13	First Pass	NC_000007.13	Chr7	19,413,271	19,547,949
nssv1418002	Submitted genomic		NC_000007.11:g.(?_ 19186511)_(1932118 9_?)dup	NCBI35 (hg17)		NC_000007.11	Chr7	19,186,511	19,321,189
nssv1418003	Submitted genomic		NC_000007.11:g.(?_ 19186511)_(1932118 9_?)dup	NCBI35 (hg17)		NC_000007.11	Chr7	19,186,511	19,321,189

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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