A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593802



Internal ID20966873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86025119..86025860hg38UCSC Ensembl
chr11:85736161..85736902hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229267
Samples
Known GenesPICALM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593802
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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