A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522705



Internal ID15103312
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706117
Samples
Known GenesRNF26
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522705
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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