A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268026



Internal ID20835066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146242590..146243185hg38UCSC Ensembl
chr5:145622153..145622748hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571352
Supporting Variants
Samples
Known GenesRBM27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268026
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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