A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592082



Internal ID16032805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155763308..155783070hg38UCSC Ensembl
Innerchr3:155481097..155500859hg19UCSC Ensembl
Innerchr3:156963791..156983553hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3819763
hg1919763
hg1819763
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8657n54
Supporting Variantsnssv976857
Samples
Known GenesC3orf33
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592082
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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