A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518382



Internal ID294771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70801151..70802270hg38UCSC Ensembl
chr15:71093490..71094609hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381120
hg191120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702358
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518382
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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