A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481161



Internal ID258655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118986509..118989368hg38UCSC Ensembl
chr9:121748787..121751646hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg382860
hg192860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481161
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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