A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266697



Internal ID20833737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134030256..134030710hg38UCSC Ensembl
chr5:133365947..133366401hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568337
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266697
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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