A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585796



Internal ID16373205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26279504..26337643hg38UCSC Ensembl
Innerchr20:26260140..26318279hg19UCSC Ensembl
Innerchr20:26208140..26266279hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3858140
hg1958140
hg1858140
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7530n54
Supporting Variantsnssv939040, nssv939042, nssv939039, nssv939041, nssv939043
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585796
Frequency
Sample Size17421
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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