A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv262n21



Internal ID22766454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44375738..44379021hg38UCSC Ensembl
chr22:44771618..44774901hg19UCSC Ensembl
chr22:43150282..43153565hg18UCSC Ensembl
chr22:43092155..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 Variants
Supporting Variantsnsv517953, nsv521348
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv262n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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