A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238279



Internal ID20805319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40819327..40820054hg38UCSC Ensembl
chr15:41111525..41112252hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588468
Supporting Variants
Samples
Known GenesPPP1R14D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238279
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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