A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239132



Internal ID20806172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97633897..97634329hg38UCSC Ensembl
chr15:98177127..98177559hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579863
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239132
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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