A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585778



Internal ID16373187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26265450..26337643hg38UCSC Ensembl
Innerchr20:26246086..26318279hg19UCSC Ensembl
Innerchr20:26194086..26266279hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3872194
hg1972194
hg1872194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7527n54
Supporting Variantsnssv939006
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585778
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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