A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500848



Internal ID277771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38532929..38533524hg38UCSC Ensembl
chr15:38825130..38825725hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701543
Samples
Known GenesRASGRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500848
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