A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100239



Internal ID21283056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73849907..73855890hg38UCSC Ensembl
Innerchr18:71517142..71523125hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg385984
hg195984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110851
Supporting Variants
Samplessample337
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100239
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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