A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103716



Internal ID22012949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1660904..1683270hg38UCSC Ensembl
chr11:1682134..1704500hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3822367
hg1922367
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584399
Samples
Known GenesFAM99A, MOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103716
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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