A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695740



Internal ID15432392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:45859124..45861475hg38UCSC Ensembl
Innerchr22:46255004..46257355hg19UCSC Ensembl
Innerchr22:44633668..44636019hg18UCSC Ensembl
Innerchr22:44575541..44577892hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg382352
hg192352
hg182352
hg172352
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518308
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695740
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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