A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593483



Internal ID20966554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94462302..94463323hg38UCSC Ensembl
chr13:95114556..95115577hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381022
hg191022
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236856
Samples
Known GenesDCT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593483
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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