A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17013426



Internal ID76627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85808800..85915222hg38UCSC Ensembl
chr8:86821029..86927451hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38106423
hg19106423
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477010
Supporting Variants
Samples
Known GenesREXO1L2P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17013426
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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