A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591769



Internal ID16379178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:131994722..132160744hg38UCSC Ensembl
Innerchr3:131713566..131879588hg19UCSC Ensembl
Innerchr3:133196256..133362278hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38166023
hg19166023
hg18166023
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv973971
Samples
Known GenesCPNE4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591769
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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