A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17014384



Internal ID77258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106981040..106981171hg38UCSC Ensembl
chr8:107993268..107993399hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476642
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17014384
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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