A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099601



Internal ID21269216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:75454522..75457261hg38UCSC Ensembl
Innerchr18:73166477..73169216hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg382740
hg192740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116003
Supporting Variants
Samplessample136
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099601
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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