A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230364



Internal ID20797404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76402428..76403098hg38UCSC Ensembl
chr11:76113472..76114142hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587609
Supporting Variants
Samples
Known GenesLOC100506127
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230364
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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