A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489755



Internal ID267026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13370379..13370984hg38UCSC Ensembl
chr10:13412379..13412984hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030264
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489755
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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