A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681125



Internal ID15417777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33220819..33224596hg38UCSC Ensembl
Innerchr22:33616805..33620582hg19UCSC Ensembl
Innerchr22:31946805..31950582hg18UCSC Ensembl
Innerchr22:31941359..31945136hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg383778
hg193778
hg183778
hg173778
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519681
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681125
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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