A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586639



Internal ID16027362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63737947..63739289hg38UCSC Ensembl
Innerchr20:62369300..62370642hg19UCSC Ensembl
Innerchr20:61839744..61841086hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381343
hg191343
hg181343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7681n54
Supporting Variantsnssv943875
Samples
Known GenesLIME1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586639
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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