A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023928



Internal ID20590968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42129212..42141617hg38UCSC Ensembl
chr15:42421410..42433815hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3812406
hg1912406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510603
Supporting Variants
Samples
Known GenesPLA2G4F
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023928
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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