A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097789



Internal ID21279735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19866890..19868956hg38UCSC Ensembl
Innerchr17:19770203..19772269hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382067
hg192067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114069
Supporting Variants
Samplessample289
Known GenesULK2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097789
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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