A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483533



Internal ID260969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25898943..25903170hg38UCSC Ensembl
chr10:26187872..26192099hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg384228
hg194228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483533
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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