A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558836



Internal ID331889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68865436..68865487hg38UCSC Ensembl
chr15:69157775..69157826hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381290
hg191290
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703934
Samples
Known GenesMIR548H4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558836
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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