A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594298



Internal ID20967369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17298988..17299668hg38UCSC Ensembl
chr11:17320535..17321215hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38681
hg19681
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219510
Samples
Known GenesNUCB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594298
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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