A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267327



Internal ID20834367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134627291..134627845hg38UCSC Ensembl
chr5:133962981..133963535hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558394
Supporting Variants
Samples
Known GenesSAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267327
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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