A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097608



Internal ID21273846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67422122..67427794hg38UCSC Ensembl
Innerchr17:65418238..65423910hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg385673
hg195673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116866
Supporting Variants
Samplessample197
Known GenesPITPNC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097608
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer