A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483093



Internal ID260536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86488214..86493275hg38UCSC Ensembl
chr10:88247971..88253032hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg385062
hg195062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038329
Samples
Known GenesWAPAL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483093
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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