A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267196



Internal ID20834236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112855244..112856148hg38UCSC Ensembl
chr5:112190941..112191845hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38905
hg19905
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568937
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267196
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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