A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534941



Internal ID231799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108471109..108471109hg38UCSC Ensembl
chr3:108189956..108189956hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16938499
Samples
Known GenesMYH15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534941
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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