A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17014575



Internal ID77388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94585428..94585465hg38UCSC Ensembl
chr8:95597656..95597693hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5549010
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17014575
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002342


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