A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585929



Internal ID16026652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33658457..33667228hg38UCSC Ensembl
Innerchr20:32246263..32255034hg19UCSC Ensembl
Innerchr20:31709924..31718695hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg388772
hg198772
hg188772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7560n54
Supporting Variantsnssv939294
Samples
Known GenesACTL10, C20orf144, NECAB3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585929
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