A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489469



Internal ID266747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75190498..75199051hg38UCSC Ensembl
chr9:77805414..77813967hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg388554
hg198554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024371
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489469
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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