A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586575



Internal ID16373984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63540916..63591039hg38UCSC Ensembl
Innerchr20:62172269..62222392hg19UCSC Ensembl
Innerchr20:61642713..61692836hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3850124
hg1950124
hg1850124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7668n54
Supporting Variantsnssv1150972
SamplesHGDP00899
Known GenesC20orf195, GMEB2, HELZ2, SRMS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586575
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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