A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098889



Internal ID21269633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:62018949..62026070hg38UCSC Ensembl
Innerchr17:60096310..60103431hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg387122
hg197122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114303
Supporting Variants
Samplessample141
Known GenesMED13
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098889
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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