A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484378



Internal ID261789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133659842..133659895hg38UCSC Ensembl
chr9:136524964..136525017hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030111
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484378
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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