A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17012769



Internal ID76184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:57729858..57733698hg38UCSC Ensembl
chr8:58642417..58646257hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg383841
hg193841
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490065
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17012769
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001249


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