A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099063



Internal ID21278416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61027801..61031801hg38UCSC Ensembl
Innerchr20:59602857..59606857hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384001
hg194001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113528
Supporting Variants
Samplessample27
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099063
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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