A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17015364



Internal ID77898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121500987..121510887hg38UCSC Ensembl
chr8:122513227..122523127hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg389901
hg199901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142228
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17015364
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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