A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228045



Internal ID20795085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91838902..91840313hg38UCSC Ensembl
chr10:93598659..93600070hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg381412
hg191412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594667
Supporting Variants
Samples
Known GenesTNKS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228045
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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