A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479580



Internal ID257099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82745490..82747054hg38UCSC Ensembl
chr9:85360405..85361969hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381565
hg191565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479580
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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