A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695074



Internal ID15431726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:33261460..33280124hg38UCSC Ensembl
Innerchr3:33302952..33321616hg19UCSC Ensembl
Innerchr3:33277956..33296620hg18UCSC Ensembl
Innerchr3:33277956..33296620hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3818665
hg1918665
hg1818665
hg1718665
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522292
Supporting Variants
Samples
Known GenesFBXL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695074
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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