A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585963



Internal ID16026686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:38088540..38228214hg38UCSC Ensembl
Innerchr20:36716942..36856616hg19UCSC Ensembl
Innerchr20:36150356..36290030hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38139675
hg19139675
hg18139675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939355
Samples
Known GenesKIAA1755, RPRD1B, TGM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585963
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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