A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939013



Internal ID16232969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26275929..26337643hg38UCSC Ensembl
Innerchr20:26256565..26318279hg19UCSC Ensembl
Innerchr20:26204565..26266279hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3861715
hg1961715
hg1861715
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585781
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv939013
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