A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267158



Internal ID20834198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:110907408..110922452hg38UCSC Ensembl
chr5:110243107..110258151hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3815045
hg1915045
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571143
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267158
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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