A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097964



Internal ID21267210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68816731..68825919hg38UCSC Ensembl
Innerchr17:66812872..66822060hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg389189
hg199189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112481
Supporting Variants
Samplessample11
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097964
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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