A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100828



Internal ID21288120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:55606250..55611408hg38UCSC Ensembl
Innerchr20:54181308..54186466hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg385159
hg195159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110328
Supporting Variants
Samplessample412
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100828
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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