A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17016712



Internal ID78796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109541203..109541329hg38UCSC Ensembl
chr8:110553432..110553558hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486904
Supporting Variants
Samples
Known GenesEBAG9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17016712
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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