A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527062



Internal ID15454355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:45622214..45627759hg38UCSC Ensembl
Innerchr22:46018094..46023639hg19UCSC Ensembl
Innerchr22:44396758..44402303hg18UCSC Ensembl
Innerchr22:44338631..44344176hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg385546
hg195546
hg185546
hg175546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703440
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527062
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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