A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155650



Internal ID22086155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16682100..16687127hg38UCSC Ensembl
Outerchr20:16681573..16689232hg38UCSC Ensembl
Innerchr20:16662745..16667772hg19UCSC Ensembl
Outerchr20:16662218..16669877hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg387660
hg197660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013881
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155650
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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