A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17012591



Internal ID76067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63287202..63288605hg38UCSC Ensembl
chr8:64199760..64201163hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg381404
hg191404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489374
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17012591
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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