A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487016



Internal ID264366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89062370..89071323hg38UCSC Ensembl
chr10:90822127..90831080hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg388954
hg198954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036387
Samples
Known GenesMIR4679-1, MIR4679-2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487016
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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