A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498340



Internal ID275332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41227087..41229215hg38UCSC Ensembl
chr15:41519285..41521413hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382129
hg192129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701104
Samples
Known GenesEXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498340
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