A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487160



Internal ID264504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63973447..63990447hg38UCSC Ensembl
chr9:69217193..69233863hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3817001
hg1916671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024045
Samples
Known GenesCBWD6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487160
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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