A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943472



Internal ID22718921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41842508..41842638hg38UCSC Ensembl
chr15:42134706..42134836hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377753
Samples
Known GenesJMJD7-PLA2G4B, PLA2G4B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943472
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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