A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152198



Internal ID15878719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47124913..47152678hg38UCSC Ensembl
Innerchr22:47520809..47548321hg19UCSC Ensembl
Innerchr22:45899473..45926985hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3827766
hg1927513
hg1827513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589140
Supporting Variants
SamplesHGDP01248
Known GenesTBC1D22A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152198
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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