A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv973613



Internal ID16267569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:131983499..131994173hg38UCSC Ensembl
Innerchr3:131702343..131713017hg19UCSC Ensembl
Innerchr3:133185033..133195707hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3810675
hg1910675
hg1810675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591726
Supporting Variants
Samples
Known GenesCPNE4, MIR5704
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv973613
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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