A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581163



Internal ID16368572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:20224214..20225195hg38UCSC Ensembl
Innerchr2:20423975..20424956hg19UCSC Ensembl
Innerchr2:20287456..20288437hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38982
hg19982
hg18982
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv904425
Samples
Known GenesSDC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581163
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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