A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239728



Internal ID20806768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78486431..78486552hg38UCSC Ensembl
chr15:78778773..78778894hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589833
Supporting Variants
Samples
Known GenesIREB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239728
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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