A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5494991



Internal ID272117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117147200..117147280hg38UCSC Ensembl
chr10:118906711..118906791hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040730
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5494991
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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