A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17017025



Internal ID79009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123810597..123810675hg38UCSC Ensembl
chr8:124822837..124822915hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480000
Supporting Variants
Samples
Known GenesFAM91A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17017025
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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