A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219597



Internal ID20786637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96798276..96799549hg38UCSC Ensembl
chr10:98558033..98559306hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381274
hg191274
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578040
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219597
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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