A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496226



Internal ID20869426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81258082..81334893hg38UCSC Ensembl
chr15:81550423..81627234hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3876812
hg1976812
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177756
Samples
Known GenesIL16, STARD5, TMC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496226
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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