A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486312



Internal ID263681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84256277..84260379hg38UCSC Ensembl
chr10:86016033..86020135hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg384103
hg194103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037241
Samples
Known GenesRGR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486312
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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