A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239631



Internal ID20806671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68932578..68933706hg38UCSC Ensembl
chr15:69224917..69226045hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381129
hg191129
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575589
Supporting Variants
Samples
Known GenesMIR548H4, NOX5, SPESP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239631
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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