A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098548



Internal ID21283642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9644661..9647006hg38UCSC Ensembl
Innerchr17:9547978..9550323hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg382346
hg192346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113515
Supporting Variants
Samplessample348
Known GenesUSP43
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098548
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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