A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580867



Internal ID18532462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:131339734..131516504hg38UCSC Ensembl
Innerchr2:132097307..132274077hg19UCSC Ensembl
Innerchr2:131813777..131990547hg18UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg38176771
hg19176771
hg18176771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010162
Supporting Variants
Samples
Known GenesLINC01120, LOC150776, LOC401010, MIR4784, MZT2A, RNU6-81P, TUBA3D, WTH3DI
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580867
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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