A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152372



Internal ID15532197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23446011..23588763hg38UCSC Ensembl
Innerchr20:23426648..23569400hg19UCSC Ensembl
Innerchr20:23374648..23517400hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38142753
hg19142753
hg18142753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585723
Supporting Variants
SamplesHGDP01273
Known GenesCST11, CST13P, CST8, CST9L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152372
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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