A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585409



Internal ID16372818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:8932617..8964988hg38UCSC Ensembl
Innerchr20:8913264..8945635hg19UCSC Ensembl
Innerchr20:8861264..8893635hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3832372
hg1932372
hg1832372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151200
Samples1780862528_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585409
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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