A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027402



Internal ID20594442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90926066..90928246hg38UCSC Ensembl
chr15:91469296..91471476hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382181
hg192181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499907
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027402
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