A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591013



Internal ID20964084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75368853..75369331hg38UCSC Ensembl
chr11:75079897..75080375hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232730
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591013
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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