A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486180



Internal ID263552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84759368..84775684hg38UCSC Ensembl
chr10:86519124..86535440hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3816317
hg1916317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038211
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486180
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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