A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489107



Internal ID266396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92835977..92836053hg38UCSC Ensembl
chr10:94595734..94595810hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037922
Samples
Known GenesEXOC6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489107
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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