A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585775



Internal ID16373184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26134874..26265450hg38UCSC Ensembl
Innerchr20:26115510..26246086hg19UCSC Ensembl
Innerchr20:26063510..26194086hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38130577
hg19130577
hg18130577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7526n54
Supporting Variantsnssv1152380
SamplesHGDP00187
Known GenesLOC284801, MIR663A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585775
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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