A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv920074



Internal ID15867344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:132495813..132657597hg38UCSC Ensembl
Innerchr2:133253386..133415170hg19UCSC Ensembl
Innerchr2:132969856..133131640hg18UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg38161785
hg19161785
hg18161785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583155
Supporting Variants
Samples
Known GenesGPR39, LYPD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv920074
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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