A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026046



Internal ID20593086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60660601..60661400hg38UCSC Ensembl
chr15:60952800..60953599hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502175
Supporting Variants
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026046
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01585


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