A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589467



Internal ID16376876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:5366617..5496330hg38UCSC Ensembl
Innerchr3:5408302..5538017hg19UCSC Ensembl
Innerchr3:5383302..5513017hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38129714
hg19129716
hg18129716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152471
SamplesHGDP00080
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589467
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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