A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941396



Internal ID15888666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54031284..54041258hg38UCSC Ensembl
Innerchr20:52647823..52657797hg19UCSC Ensembl
Innerchr20:52081230..52091204hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg389975
hg199975
hg189975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586244
Supporting Variants
Samples
Known GenesBCAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv941396
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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