A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17018848



Internal ID80197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4735269..4735408hg38UCSC Ensembl
chr9:4735269..4735408hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487179
Supporting Variants
Samples
Known GenesAK3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17018848
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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