A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225674



Internal ID20792714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113616283..113617053hg38UCSC Ensembl
chr11:113487005..113487775hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38771
hg19771
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590819
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225674
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00022


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