A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238876



Internal ID20805916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65168353..65169046hg38UCSC Ensembl
chr15:65460691..65461384hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579179
Supporting Variants
Samples
Known GenesCLPX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238876
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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