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dbVar

Database of genomic structural variation

nsv499463

Organism: Homo sapiens

Study:nstd47 (Kidd et al. 2010b)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:582

Publication(s):Kidd et al. 2010

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: 179 SVs from 42 studies. See in: genome view

Remapped(Score: Perfect):73,129,297-73,129,878

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv499463	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	73,129,297	73,129,878
nsv499463	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	73,594,980	73,595,561
nsv499463	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000001.9	Chr1	73,367,568	73,368,149

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv586157	copy number gain	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv586157	Remapped	Perfect	NC_000001.11:g.731 29297_73129878dup	GRCh38.p12	First Pass	NC_000001.11	Chr1	73,129,297	73,129,878
nssv586157	Remapped	Perfect	NC_000001.10:g.735 94980_73595561dup	GRCh37.p13	First Pass	NC_000001.10	Chr1	73,594,980	73,595,561
nssv586157	Submitted genomic		NC_000001.9:g.7336 7568_73368149dup	NCBI36 (hg18)		NC_000001.9	Chr1	73,367,568	73,368,149

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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