A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14084569



Internal ID21274142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66125246..66128189hg38UCSC Ensembl
Innerchr7:65590233..65593176hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382944
hg192944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111195
Supporting Variants
Samplessample202
Known GenesCRCP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14084569
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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