A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484222



Internal ID261640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:64131317..64132668hg38UCSC Ensembl
chr10:65891078..65892429hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381352
hg191352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035927
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484222
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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