A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476419



Internal ID254030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24730534..24770488hg38UCSC Ensembl
chr10:25019463..25059417hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3839955
hg1939955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476419
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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