A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937958



Internal ID22713333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41847301..41847472hg38UCSC Ensembl
chr15:42139499..42139670hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376997
Samples
Known GenesJMJD7-PLA2G4B, PLA2G4B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937958
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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