A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228880



Internal ID20795920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59583157..59583634hg38UCSC Ensembl
chr11:59350630..59351107hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581514
Supporting Variants
Samples
Known GenesOSBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228880
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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