A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013661



Internal ID19102880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34427331..34512953hg38UCSC Ensembl
Innerchr2:34652398..34738020hg19UCSC Ensembl
Innerchr2:34505902..34591524hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3885623
hg1985623
hg1885623
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3758n100
Supporting Variantsnssv3580902, nssv3728008, nssv3580901
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013661
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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