A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269106



Internal ID20836146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56013710..56016275hg38UCSC Ensembl
chr5:55309538..55312103hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg382566
hg192566
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567248
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269106
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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