A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586614



Internal ID16027337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63725275..63741460hg38UCSC Ensembl
Innerchr20:62356627..62372813hg19UCSC Ensembl
Innerchr20:61827071..61843257hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3816186
hg1916187
hg1816187
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv943842
Samples
Known GenesLIME1, SLC2A4RG, ZGPAT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586614
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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