A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584812



Internal ID16372221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240616574..240639691hg38UCSC Ensembl
Innerchr2:241555991..241579108hg19UCSC Ensembl
Innerchr2:241204664..241227781hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3823118
hg1923118
hg1823118
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv933827, nssv933828
Samples
Known GenesGPR35
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584812
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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