A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594771



Internal ID20967842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86399605..86400108hg38UCSC Ensembl
chr11:86110647..86111150hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222811
Samples
Known GenesCCDC81
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594771
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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