A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585290



Internal ID16372699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3835007..3843810hg38UCSC Ensembl
Innerchr20:3815654..3824457hg19UCSC Ensembl
Innerchr20:3763654..3772457hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg388804
hg198804
hg188804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7443n54
Supporting Variantsnssv937357, nssv937358
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585290
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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