A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097955



Internal ID21291168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67422824..67428559hg38UCSC Ensembl
Innerchr17:65418940..65424675hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg385736
hg195736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115534
Supporting Variants
Samplessample7
Known GenesPITPNC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097955
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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