A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594498



Internal ID20967569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47421211..47421683hg38UCSC Ensembl
chr11:47442762..47443234hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223689
Samples
Known GenesPSMC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594498
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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