A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025417



Internal ID84679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83804122..83804397hg38UCSC Ensembl
chr9:86419037..86419312hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474793
Supporting Variants
Samples
Known GenesGKAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025417
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001562


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