A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17014659



Internal ID77439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97592222..97620222hg38UCSC Ensembl
chr8:98604450..98632450hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3828001
hg1928001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142206
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17014659
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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