A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493917



Internal ID271080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118345928..118347444hg38UCSC Ensembl
chr10:120105440..120106956hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381517
hg191517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040795
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493917
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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