A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246769



Internal ID20813809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23122051..23123217hg38UCSC Ensembl
chr18:20702015..20703181hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381167
hg191167
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593431
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246769
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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