A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676520



Internal ID15066486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:19729797..19750832hg38UCSC Ensembl
Innerchr22:19717320..19738355hg19UCSC Ensembl
Innerchr22:18097320..18118355hg18UCSC Ensembl
Innerchr22:18091874..18112909hg17UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3821036
hg1921036
hg1821036
hg1721036
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517478
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676520
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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