A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485168



Internal ID262565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92191074..92191961hg38UCSC Ensembl
chr9:94953356..94954243hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38888
hg19888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027399
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485168
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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