A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270276



Internal ID20837316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78686502..78940875hg38UCSC Ensembl
chr5:77982325..78236698hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38254374
hg19254374
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560635
Supporting Variants
Samples
Known GenesARSB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270276
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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