A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585983



Internal ID16373392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:40040435..40082820hg38UCSC Ensembl
Innerchr20:38669077..38711461hg19UCSC Ensembl
Innerchr20:38102491..38144875hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3842386
hg1942385
hg1842385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939404
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585983
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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