A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594428



Internal ID20967499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94121081..94123713hg38UCSC Ensembl
chr11:93854247..93856879hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382633
hg192633
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594428
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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