A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522692



Internal ID15449985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:44534821..44535712hg38UCSC Ensembl
Innerchr22:44930701..44931592hg19UCSC Ensembl
Innerchr22:43309365..43310256hg18UCSC Ensembl
Innerchr22:43251238..43252129hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38892
hg19892
hg18892
hg17892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706102
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522692
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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