A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17590936



Internal ID21782979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94808316..94812412hg38UCSC Ensembl
chr11:94541482..94545578hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg384097
hg194097
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110726
Supporting Variants
Samples
Known GenesAMOTL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17590936
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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