A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220229



Internal ID20787269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27747107..27747817hg38UCSC Ensembl
chr11:27768654..27769364hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580501
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220229
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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