A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586581



Internal ID20959652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:761046..762267hg38UCSC Ensembl
chr11:761046..762267hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381222
hg191222
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219337
Samples
Known GenesTALDO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586581
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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