A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026201



Internal ID20593241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58921901..58923600hg38UCSC Ensembl
chr15:59214100..59215799hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503093
Supporting Variants
Samples
Known GenesSLTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026201
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