A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580623



Internal ID20953694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50018910..50024477hg38UCSC Ensembl
chr13:50593046..50598613hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg385568
hg195568
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221728
Samples
Known GenesDLEU2, KCNRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580623
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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