A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676752



Internal ID15066718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:20977267..20992430hg38UCSC Ensembl
Innerchr22:21331556..21346719hg19UCSC Ensembl
Innerchr22:19661556..19676719hg18UCSC Ensembl
Innerchr22:19656110..19671273hg17UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3815164
hg1915164
hg1815164
hg1715164
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520145
Supporting Variants
Samples
Known GenesAIFM3, LZTR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676752
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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