A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522451



Internal ID15103058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:23387511..23399918hg38UCSC Ensembl
Innerchr22:23729698..23742105hg19UCSC Ensembl
Innerchr22:22059698..22072105hg18UCSC Ensembl
Innerchr22:22054252..22066659hg17UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3812408
hg1912408
hg1812408
hg1712408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705812
Samples
Known GenesZDHHC8P1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522451
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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