A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592140



Internal ID20965211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111263458..111264361hg38UCSC Ensembl
chr11:111134183..111135086hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38904
hg19904
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220928
Samples
Known GenesC11orf53
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592140
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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