A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086658



Internal ID21282207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66125246..66128201hg38UCSC Ensembl
Innerchr7:65590233..65593188hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382956
hg192956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112681
Supporting Variants
Samplessample322
Known GenesCRCP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086658
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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