A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233572



Internal ID20800612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18348964..18349621hg38UCSC Ensembl
chr11:18370511..18371168hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584931
Supporting Variants
Samples
Known GenesGTF2H1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233572
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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