A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17009099



Internal ID73702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19758314..19759691hg38UCSC Ensembl
chr8:19615825..19617202hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg381378
hg191378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491309
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17009099
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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