A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098652



Internal ID21286626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67423128..67430121hg38UCSC Ensembl
Innerchr17:65419244..65426237hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg386994
hg196994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113832
Supporting Variants
Samplessample391
Known GenesPITPNC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098652
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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