A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv943839



Internal ID15891109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63680946..63709340hg38UCSC Ensembl
Innerchr20:62312299..62340692hg19UCSC Ensembl
Innerchr20:61782743..61811136hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3828395
hg1928394
hg1828394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586611
Supporting Variants
Samples
Known GenesARFRP1, RTEL1, RTEL1-TNFRSF6B, TNFRSF6B, ZGPAT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv943839
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