A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227998



Internal ID20795038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86730889..86731367hg38UCSC Ensembl
chr10:88490646..88491124hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594431
Supporting Variants
Samples
Known GenesLDB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227998
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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