A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528344



Internal ID15455637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21691314..21692498hg38UCSC Ensembl
Innerchr22:22045603..22046787hg19UCSC Ensembl
Innerchr22:20375603..20376787hg18UCSC Ensembl
Innerchr22:20370157..20371341hg17UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg381185
hg191185
hg181185
hg171185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704927
Samples
Known GenesPPIL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528344
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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