A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589236



Internal ID16029959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:31065..140991hg38UCSC Ensembl
Innerchr3:72739..182674hg19UCSC Ensembl
Innerchr3:47739..157674hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38109927
hg19109936
hg18109936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8142n54
Supporting Variantsnssv1152220
SamplesHGDP00096
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589236
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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