A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270283



Internal ID20837323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78998927..78999283hg38UCSC Ensembl
chr5:78294750..78295106hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574007
Supporting Variants
Samples
Known GenesDMGDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270283
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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