A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231301



Internal ID20798341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93722225..93722817hg38UCSC Ensembl
chr11:93455391..93455983hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582154
Supporting Variants
Samples
Known GenesKIAA1731
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231301
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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