A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586502



Internal ID16373911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62645662..62678188hg38UCSC Ensembl
Innerchr20:61277014..61309540hg19UCSC Ensembl
Innerchr20:60747459..60779985hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3832527
hg1932527
hg1832527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv942125
Samples
Known GenesLOC100127888, SLCO4A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586502
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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