A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232046



Internal ID20799086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100211914..100212785hg38UCSC Ensembl
chr10:101971671..101972542hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38872
hg19872
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581953
Supporting Variants
Samples
Known GenesCHUK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232046
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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