A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231943



Internal ID20798983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57748093..57748426hg38UCSC Ensembl
chr11:57515565..57515898hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578921
Supporting Variants
Samples
Known GenesBTBD18, TMX2-CTNND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231943
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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