A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521348



Internal ID15448641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:44375738..44379021hg38UCSC Ensembl
Innerchr22:44771618..44774901hg19UCSC Ensembl
Innerchr22:43150282..43153565hg18UCSC Ensembl
Innerchr22:43092155..43095438hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg383284
hg193284
hg183284
hg173284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv262n21
Supporting Variantsnssv697958
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521348
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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