A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227982



Internal ID20795022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101151024..101151107hg38UCSC Ensembl
chr11:101021755..101021838hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582491
Supporting Variants
Samples
Known GenesLOC101054525
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227982
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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