A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191961



Internal ID20759001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42011068..42133627hg38UCSC Ensembl
chr15:42303266..42425825hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38122560
hg19122560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496869
Supporting Variants
Samples
Known GenesPLA2G4D, PLA2G4E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191961
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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