A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498876



Internal ID275859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124052941..124053023hg38UCSC Ensembl
chr10:125812457..125812539hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040486
Samples
Known GenesCHST15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498876
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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