A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491125



Internal ID268369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52484043..52489015hg38UCSC Ensembl
chr10:54243803..54248775hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg384973
hg194973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17034773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491125
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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