A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246844



Internal ID20813885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25973697..25975262hg38UCSC Ensembl
chr18:23553661..23555226hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381566
hg191566
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591411
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246844
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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