A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099718



Internal ID21289313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61018157..61031801hg38UCSC Ensembl
Innerchr20:59593213..59606857hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3813645
hg1913645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117737
Supporting Variants
Samplessample45
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099718
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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