A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496675



Internal ID20869878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55473734..55476208hg38UCSC Ensembl
chr15:55765932..55768406hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg382475
hg192475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024844
Samples
Known GenesDYX1C1, DYX1C1-CCPG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496675
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