A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592617



Internal ID16033340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176334223..176558782hg38UCSC Ensembl
Innerchr3:176052011..176276570hg19UCSC Ensembl
Innerchr3:177534705..177759264hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38224560
hg19224560
hg18224560
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152883
SamplesHGDP00988
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592617
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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