A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938972



Internal ID15886242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:24951392..25026453hg38UCSC Ensembl
Innerchr20:24932028..25007089hg19UCSC Ensembl
Innerchr20:24880028..24955089hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3875062
hg1975062
hg1875062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585745
Supporting Variants
Samples
Known GenesACSS1, APMAP, CST7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv938972
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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