A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706117



Internal ID15096083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119335120..119337218hg38UCSC Ensembl
Innerchr11:119205830..119207928hg19UCSC Ensembl
Innerchr11:118711040..118713138hg18UCSC Ensembl
Innerchr11:118711040..118713138hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382099
hg192099
hg182099
hg172099
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522705
Supporting Variants
Samples
Known GenesRNF26
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706117
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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