A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190373



Internal ID20757413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43624901..43659400hg38UCSC Ensembl
chr15:43917099..43951598hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3834500
hg1934500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511355
Supporting Variants
Samples
Known GenesCATSPER2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190373
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00671


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