A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063102



Internal ID19152321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:46994239..47016554hg38UCSC Ensembl
Innerchr22:47390135..47412450hg19UCSC Ensembl
Innerchr22:45768799..45791114hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3822316
hg1922316
hg1822316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3592267
Samples
Known GenesTBC1D22A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063102
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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