A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941779



Internal ID15889049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:57525705..57527189hg38UCSC Ensembl
Innerchr20:56100761..56102245hg19UCSC Ensembl
Innerchr20:55534167..55535651hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg381485
hg191485
hg181485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586341
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv941779
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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