A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025748



Internal ID20592788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75869480..75869847hg38UCSC Ensembl
chr15:76161821..76162188hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498060
Supporting Variants
Samples
Known GenesUBE2Q2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025748
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00065


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