A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586129



Internal ID16026852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45726581..45749938hg38UCSC Ensembl
Innerchr20:44355220..44378577hg19UCSC Ensembl
Innerchr20:43788634..43811984hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3823358
hg1923358
hg1823351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7592n54
Supporting Variantsnssv1150952, nssv1150954, nssv1150951, nssv1150949, nssv1150953, nssv1150950
SamplesHGDP00795, HGDP00797, HGDP00806, HGDP00799, HGDP01079, HGDP01376
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586129
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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