A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528985



Internal ID15456278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:37675036..37695653hg38UCSC Ensembl
Innerchr22:38071043..38091660hg19UCSC Ensembl
Innerchr22:36400989..36421606hg18UCSC Ensembl
Innerchr22:36395543..36416160hg17UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3820618
hg1920618
hg1820618
hg1720618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705685
Samples
Known GenesLGALS1, NOL12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528985
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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