A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152883



Internal ID15530741
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 StatusS
Merged Variantsnsv592617
Supporting Variants
SamplesHGDP00988
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152883
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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