A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556052



Internal ID329197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77490874..77490925hg38UCSC Ensembl
chr15:77783216..77783267hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702131
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556052
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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