A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098096



Internal ID21291204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:53365580..53369980hg38UCSC Ensembl
Innerchr17:51442941..51447341hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg384401
hg194401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116737
Supporting Variants
Samplessample70
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098096
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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