A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238002



Internal ID20805042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38737841..38739213hg38UCSC Ensembl
chr15:39030042..39031414hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381373
hg191373
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586136
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238002
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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