A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231055



Internal ID20798095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71961357..71962056hg38UCSC Ensembl
chr11:71672403..71673102hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581552
Supporting Variants
Samples
Known GenesRNF121
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231055
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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