A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680070



Internal ID15416722
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516494
Supporting Variants
Samples
Known GenesCPNE4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680070
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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