A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023651



Internal ID20590691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41167197..41172856hg38UCSC Ensembl
chr15:41459395..41465054hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg385660
hg195660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511601
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023651
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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