A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489016



Internal ID266309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107731893..107732019hg38UCSC Ensembl
chr9:110494174..110494300hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489016
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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