A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592604



Internal ID16380013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176088947..176178790hg38UCSC Ensembl
Innerchr3:175806735..175896578hg19UCSC Ensembl
Innerchr3:177289429..177379272hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3889844
hg1989844
hg1889844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8747n54
Supporting Variantsnssv981608
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592604
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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