A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663377



Internal ID15400029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:46984564..46995414hg38UCSC Ensembl
Innerchr22:47380460..47391310hg19UCSC Ensembl
Innerchr22:45759124..45769974hg18UCSC Ensembl
Innerchr22:45700979..45711829hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3810851
hg1910851
hg1810851
hg1710851
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519607
Supporting Variants
Samples
Known GenesTBC1D22A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663377
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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