A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17017954



Internal ID79620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116301750..116301801hg38UCSC Ensembl
chr8:117313988..117314039hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5399364
Supporting Variants
Samples
Known GenesLINC00536
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17017954
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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