A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268046



Internal ID20835086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146505050..146505857hg38UCSC Ensembl
chr5:145884613..145885420hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38808
hg19808
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558109
Supporting Variants
Samples
Known GenesTCERG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268046
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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