A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481388



Internal ID258870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77675483..77675900hg38UCSC Ensembl
chr9:80290399..80290816hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025980
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481388
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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