A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279238



Internal ID20846278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9823508..9825296hg38UCSC Ensembl
chr8:9681018..9682806hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381789
hg191789
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574191
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279238
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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