A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086694



Internal ID21282866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66305542..66309411hg38UCSC Ensembl
Innerchr7:65770529..65774398hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg383870
hg193870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110202
Supporting Variants
Samplessample332
Known GenesTPST1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086694
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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