A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510042



Internal ID286672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37318550..37321414hg38UCSC Ensembl
chr15:37610751..37613615hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg382865
hg192865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv168n206
Supporting Variantsnssv17701486
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510042
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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