A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235114



Internal ID20802154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76538513..76538724hg38UCSC Ensembl
chr11:76249557..76249768hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576156
Supporting Variants
Samples
Known GenesC11orf30
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235114
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00031


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