A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592083



Internal ID16032806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155766336..155780522hg38UCSC Ensembl
Innerchr3:155484125..155498311hg19UCSC Ensembl
Innerchr3:156966819..156981005hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3814187
hg1914187
hg1814187
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8657n54
Supporting Variantsnssv976858
Samples
Known GenesC3orf33
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592083
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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