A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151732



Internal ID15879166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:27364125..27469383hg38UCSC Ensembl
Innerchr22:27760086..27865344hg19UCSC Ensembl
Innerchr22:26090086..26195344hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38105259
hg19105259
hg18105259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588875
Supporting Variants
SamplesHGDP01320
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151732
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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