A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516494



Internal ID15443787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:131741595..131778163hg38UCSC Ensembl
Innerchr3:131460439..131497007hg19UCSC Ensembl
Innerchr3:132943129..132979697hg18UCSC Ensembl
Innerchr3:132943137..132979705hg17UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3836569
hg1936569
hg1836569
hg1736569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv668680, nssv680070
Samples
Known GenesCPNE4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516494
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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