A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481336



Internal ID258822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25973202..25983950hg38UCSC Ensembl
chr10:26262131..26272879hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3810749
hg1910749
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032267
Samples
Known GenesMYO3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481336
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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