A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586504



Internal ID16373913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62658391..62688263hg38UCSC Ensembl
Innerchr20:61289743..61319615hg19UCSC Ensembl
Innerchr20:60760188..60790060hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3829873
hg1929873
hg1829873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv942127
Samples
Known GenesLOC100127888, SLCO4A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586504
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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