A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696018



Internal ID15432670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37473850..37475971hg38UCSC Ensembl
Innerchr3:37515341..37517462hg19UCSC Ensembl
Innerchr3:37490345..37492466hg18UCSC Ensembl
Innerchr3:37490345..37492466hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382122
hg192122
hg182122
hg172122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518574
Supporting Variants
Samples
Known GenesITGA9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696018
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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