A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17011312



Internal ID75188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33755694..33755733hg38UCSC Ensembl
chr8:33613212..33613251hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547535
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17011312
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003123


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