A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266164



Internal ID20833204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119039632..119040550hg38UCSC Ensembl
chr5:118375327..118376245hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557377
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266164
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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