A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586638



Internal ID16374047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63737808..63740448hg38UCSC Ensembl
Innerchr20:62369161..62371801hg19UCSC Ensembl
Innerchr20:61839605..61842245hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382641
hg192641
hg182641
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7679n54
Supporting Variantsnssv943874
Samples
Known GenesLIME1, SLC2A4RG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586638
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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