A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583388



Internal ID20956459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117150858..117151297hg38UCSC Ensembl
chr11:117021574..117022013hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228116
Samples
Known GenesPAFAH1B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583388
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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