A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584509



Internal ID20957580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117856557..117860923hg38UCSC Ensembl
chr11:117727272..117731638hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg384367
hg194367
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230551
Samples
Known GenesFXYD6, FXYD6-FXYD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584509
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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