A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17017953



Internal ID79619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116297439..116298970hg38UCSC Ensembl
chr8:117309677..117311208hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg381532
hg191532
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474820
Supporting Variants
Samples
Known GenesLINC00536
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17017953
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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