A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585984



Internal ID16373393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:40424851..40527533hg38UCSC Ensembl
Innerchr20:39053491..39156173hg19UCSC Ensembl
Innerchr20:38486905..38589587hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38102683
hg19102683
hg18102683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939405
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585984
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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