A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17013909



Internal ID76951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81466222..81470247hg38UCSC Ensembl
chr8:82378457..82382482hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg384026
hg194026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479516
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17013909
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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