A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025051



Internal ID20592092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53905801..53911200hg38UCSC Ensembl
chr15:54197998..54203397hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500361
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02836


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