A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702864



Internal ID15092830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33808943..33825972hg38UCSC Ensembl
Innerchr22:34204930..34221959hg19UCSC Ensembl
Innerchr22:32534930..32551959hg18UCSC Ensembl
Innerchr22:32529484..32546513hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3817030
hg1917030
hg1817030
hg1717030
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526550
Supporting Variants
Samples
Known GenesLARGE
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702864
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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