A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089351



Internal ID21998584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84191990..84191990hg38UCSC Ensembl
chr11:83903033..83903033hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592285
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089351
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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