A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv940977



Internal ID15888247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:48652999..48736569hg38UCSC Ensembl
Innerchr20:47269537..47353106hg19UCSC Ensembl
Innerchr20:46702944..46786513hg18UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3883571
hg1983570
hg1883570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586170
Supporting Variants
Samples
Known GenesPREX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv940977
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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