A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592605



Internal ID16380014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176114086..176183792hg38UCSC Ensembl
Innerchr3:175831874..175901580hg19UCSC Ensembl
Innerchr3:177314568..177384274hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3869707
hg1969707
hg1869707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8747n54
Supporting Variantsnssv981609
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592605
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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