A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221972



Internal ID20789012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78096474..78096826hg38UCSC Ensembl
chr11:77807520..77807872hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585666
Supporting Variants
Samples
Known GenesRNU6-83P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221972
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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