A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484834



Internal ID262239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74841080..74841187hg38UCSC Ensembl
chr10:76600838..76600945hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037070
Samples
Known GenesKAT6B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484834
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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