A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486699



Internal ID264057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90751575..90751631hg38UCSC Ensembl
chr9:93513857..93513913hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024021
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486699
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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