A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585927



Internal ID16026650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33656331..33663590hg38UCSC Ensembl
Innerchr20:32244137..32251396hg19UCSC Ensembl
Innerchr20:31707798..31715057hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg387260
hg197260
hg187260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939290, nssv939289, nssv939292, nssv939291
Samples
Known GenesC20orf144, NECAB3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585927
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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