A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580664



Internal ID20953735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99840591..99841407hg38UCSC Ensembl
chr13:100492845..100493661hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227567
Samples
Known GenesCLYBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580664
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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