A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493706



Internal ID270875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99728233..99730847hg38UCSC Ensembl
chr10:101487990..101490604hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg382615
hg192615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039848
Samples
Known GenesCOX15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493706
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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