A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269080



Internal ID20836120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55195927..55196538hg38UCSC Ensembl
chr5:54491755..54492366hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567424
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269080
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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