A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232860



Internal ID20799901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83074772..83077089hg38UCSC Ensembl
chr11:82785814..82788131hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382318
hg192318
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592728
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232860
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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