A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239658



Internal ID20806698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71491848..71492400hg38UCSC Ensembl
chr15:71784187..71784739hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594817
Supporting Variants
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239658
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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