A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100460



Internal ID22009693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26669187..26669187hg38UCSC Ensembl
chr11:26690734..26690734hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593984
Samples
Known GenesSLC5A12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100460
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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