A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098656



Internal ID21286661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67422122..67424275hg38UCSC Ensembl
Innerchr17:65418238..65420391hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg382154
hg192154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113185
Supporting Variants
Samplessample392
Known GenesPITPNC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098656
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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