A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692083



Internal ID15082049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:50026067..50032087hg38UCSC Ensembl
Innerchr22:50464496..50470516hg19UCSC Ensembl
Innerchr22:48806623..48812643hg18UCSC Ensembl
Innerchr22:48766953..48772973hg17UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg386021
hg196021
hg186021
hg176021
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516273
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692083
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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