A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658842



Internal ID15395494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65207571..65226921hg38UCSC Ensembl
Innerchr3:65193246..65212596hg19UCSC Ensembl
Innerchr3:65168286..65187636hg18UCSC Ensembl
Innerchr3:65168286..65187636hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3819351
hg1919351
hg1819351
hg1719351
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516641
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658842
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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