A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17015212



Internal ID77799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:111215556..111321603hg38UCSC Ensembl
chr8:112227785..112333832hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38106048
hg19106048
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17015212
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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