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dbVar

Database of genomic structural variation

nsv499168

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:4

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

Remapped(Score: Perfect):24,980,781-24,980,784

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv499168	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000009.12	Chr9	24,980,781	24,980,784
nsv499168	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	24,980,779	24,980,782
nsv499168	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000009.10	Chr9	24,970,779	24,970,782

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv586548	copy number gain	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv586548	Remapped	Perfect	NC_000009.12:g.249 80781_24980784dup	GRCh38.p12	First Pass	NC_000009.12	Chr9	24,980,781	24,980,784
nssv586548	Remapped	Perfect	NC_000009.11:g.249 80779_24980782dup	GRCh37.p13	First Pass	NC_000009.11	Chr9	24,980,779	24,980,782
nssv586548	Submitted genomic		NC_000009.10:g.249 70779_24970782dup	NCBI36 (hg18)		NC_000009.10	Chr9	24,970,779	24,970,782

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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