A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551798



Internal ID325222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117485560..117485591hg38UCSC Ensembl
chr10:119245071..119245102hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040746
Samples
Known GenesEMX2OS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551798
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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