A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579160



Internal ID20952231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59708459..59709467hg38UCSC Ensembl
chr11:59475932..59476940hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381009
hg191009
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223175
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579160
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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