A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233264



Internal ID20800304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66134935..66135664hg38UCSC Ensembl
chr11:65902406..65903135hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588123
Supporting Variants
Samples
Known GenesPACS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233264
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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