A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266986



Internal ID20834026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69107813..69108579hg38UCSC Ensembl
chr5:68403640..68404406hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38767
hg19767
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560182
Supporting Variants
Samples
Known GenesSLC30A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266986
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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