A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244849



Internal ID20811889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78354961..78401294hg38UCSC Ensembl
chr18:76114961..76161294hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3846334
hg1946334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595922
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244849
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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