A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100665



Internal ID21279728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:35960089..35973302hg38UCSC Ensembl
Innerchr20:34548011..34561224hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3813214
hg1913214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111261
Supporting Variants
Samplessample289
Known GenesCNBD2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100665
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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