A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656563



Internal ID15393215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25112236..25271637hg38UCSC Ensembl
Innerchr11:25133782..25293183hg19UCSC Ensembl
Innerchr11:25090358..25249759hg18UCSC Ensembl
Innerchr11:25090358..25249759hg17UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38159402
hg19159402
hg18159402
hg17159402
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516879
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656563
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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