A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524156



Internal ID15104763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33749609..33864750hg38UCSC Ensembl
Innerchr22:34145596..34260738hg19UCSC Ensembl
Innerchr22:32475596..32590738hg18UCSC Ensembl
Innerchr22:32470150..32585292hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38115142
hg19115143
hg18115143
hg17115143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700035
Samples
Known GenesLARGE, LARGE-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524156
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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