A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17021556



Internal ID82018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35228468..35228568hg38UCSC Ensembl
chr9:35228465..35228565hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475463
Supporting Variants
Samples
Known GenesUNC13B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17021556
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002967


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