A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579186



Internal ID20952257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66498362..66500188hg38UCSC Ensembl
chr11:66265833..66267659hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381827
hg191827
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235277
Samples
Known GenesDPP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579186
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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