A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520145



Internal ID15100752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:20977267..20997831hg38UCSC Ensembl
Innerchr22:21331556..21352120hg19UCSC Ensembl
Innerchr22:19661556..19682120hg18UCSC Ensembl
Innerchr22:19656110..19676674hg17UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3820565
hg1920565
hg1820565
hg1720565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv679435, nssv683783, nssv661206, nssv677475, nssv676752
Samples
Known GenesAIFM3, LZTR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520145
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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