A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17013190



Internal ID76469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76097350..76116625hg38UCSC Ensembl
chr8:77009585..77028860hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3819276
hg1919276
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484604
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17013190
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00188


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