A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585284



Internal ID16026007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3705789..3756848hg38UCSC Ensembl
Innerchr20:3686436..3737495hg19UCSC Ensembl
Innerchr20:3634436..3685495hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3851060
hg1951060
hg1851060
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937349
Samples
Known GenesC20orf27, HSPA12B, SIGLEC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585284
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer