A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587209



Internal ID20960280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92674172..92674560hg38UCSC Ensembl
chr11:92407338..92407726hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232938
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587209
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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