A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239151



Internal ID20806191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98601171..98602847hg38UCSC Ensembl
chr15:99144400..99146076hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381677
hg191677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579533
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239151
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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