A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486313



Internal ID263682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86400699..86407362hg38UCSC Ensembl
chr10:88160456..88167119hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg386664
hg196664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038318
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486313
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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