A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474219



Internal ID251883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27777601..27777694hg38UCSC Ensembl
chr10:28066530..28066623hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474219
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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