A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560242



Internal ID333254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99731565..99947520hg38UCSC Ensembl
chr15:100271770..100487725hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38215956
hg19215956
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703787
Samples
Known GenesDNM1P46, LYSMD4
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560242
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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