A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226880



Internal ID20793920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32143479..32145749hg38UCSC Ensembl
chr11:32165025..32167295hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382271
hg192271
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584023
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226880
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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