A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592081



Internal ID16032804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155763308..155776126hg38UCSC Ensembl
Innerchr3:155481097..155493915hg19UCSC Ensembl
Innerchr3:156963791..156976609hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3812819
hg1912819
hg1812819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv976856
Samples
Known GenesC3orf33
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592081
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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