A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693380



Internal ID15083346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:133680858..133692380hg38UCSC Ensembl
Innerchr3:133399702..133411224hg19UCSC Ensembl
Innerchr3:134882392..134893914hg18UCSC Ensembl
Innerchr3:134882400..134893922hg17UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3811523
hg1911523
hg1811523
hg1711523
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516081
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693380
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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