A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521128



Internal ID15448421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38879995..38885631hg38UCSC Ensembl
Innerchr22:39276000..39281636hg19UCSC Ensembl
Innerchr22:37605946..37611582hg18UCSC Ensembl
Innerchr22:37600500..37606136hg17UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg385637
hg195637
hg185637
hg175637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694083
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521128
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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