A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511488



Internal ID20884816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91965747..92080959hg38UCSC Ensembl
chr15:92508977..92624189hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38115213
hg19115213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027273
Samples
Known GenesSLCO3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511488
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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