A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591388



Internal ID20964459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66787188..66787401hg38UCSC Ensembl
chr11:66554659..66554872hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219899
Samples
Known GenesC11orf80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591388
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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