A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523770



Internal ID15451063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:44550641..44552217hg38UCSC Ensembl
Innerchr22:44946521..44948097hg19UCSC Ensembl
Innerchr22:43325185..43326761hg18UCSC Ensembl
Innerchr22:43267058..43268634hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381577
hg191577
hg181577
hg171577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699592
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523770
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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