A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481268



Internal ID258756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102183582..102215274hg38UCSC Ensembl
chr10:103943339..103975031hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3831693
hg1931693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17683819
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481268
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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