A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005928



Internal ID19095146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34423619..34512477hg38UCSC Ensembl
Innerchr2:34648686..34737544hg19UCSC Ensembl
Innerchr2:34502190..34591048hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3888859
hg1988859
hg1888859
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3758n100
Supporting Variantsnssv3580896
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)nsv1005928
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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