A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238820



Internal ID20805860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64358794..64359710hg38UCSC Ensembl
chr15:64650993..64651909hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578280
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238820
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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