A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239632



Internal ID20806672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69051563..69052140hg38UCSC Ensembl
chr15:69343903..69344480hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581244
Supporting Variants
Samples
Known GenesMIR548H4, NOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239632
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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