A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585203



Internal ID16372612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1259229..1262408hg38UCSC Ensembl
Innerchr20:1239873..1243052hg19UCSC Ensembl
Innerchr20:1187873..1191052hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383180
hg193180
hg183180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7426n54
Supporting Variantsnssv935353
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585203
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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