A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590517



Internal ID20963588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49729704..49730822hg38UCSC Ensembl
chr13:50303840..50304958hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg381119
hg191119
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230686
Samples
Known GenesKPNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590517
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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