A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939406



Internal ID16233362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:40649002..40670812hg38UCSC Ensembl
Innerchr20:39277642..39299452hg19UCSC Ensembl
Innerchr20:38711056..38732866hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3821811
hg1921811
hg1821811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585985
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv939406
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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