A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027242



Internal ID20594282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84991901..84993200hg38UCSC Ensembl
chr15:85535132..85536431hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510951
Supporting Variants
Samples
Known GenesPDE8A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027242
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