A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490298



Internal ID267557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15233786..15234132hg38UCSC Ensembl
chr9:15233784..15234130hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020586
Samples
Known GenesTTC39B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490298
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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