A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714253



Internal ID137919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69113980..69123490hg38UCSC Ensembl
chr17:67110121..67119631hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg389511
hg199511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519422
Supporting Variants
Samples
Known GenesABCA6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714253
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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