A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5494993



Internal ID272119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40119938..40130497hg38UCSC Ensembl
chr15:40412139..40422698hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3810560
hg1910560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700104
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5494993
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer