A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594119



Internal ID20967190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106616927..106617344hg38UCSC Ensembl
chr11:106487654..106488071hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233547
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594119
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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