A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377753



Internal ID22435623
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 StatusS
Merged Variantsnsv5943472
Supporting Variants
Samples
Known GenesJMJD7-PLA2G4B, PLA2G4B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377753
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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