A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230819



Internal ID20797859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9350376..9352958hg38UCSC Ensembl
chr11:9371923..9374505hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382583
hg192583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589431
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230819
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00019


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