A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218218



Internal ID20785258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18317020..18317447hg38UCSC Ensembl
chr11:18338567..18338994hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578664
Supporting Variants
Samples
Known GenesHPS5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218218
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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