A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223828



Internal ID20790868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89721658..89721931hg38UCSC Ensembl
chr10:91481415..91481688hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583036
Supporting Variants
Samples
Known GenesKIF20B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223828
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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