A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267223



Internal ID20834263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113417470..113417656hg38UCSC Ensembl
chr5:112753167..112753353hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574703
Supporting Variants
Samples
Known GenesMCC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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