A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033569



Internal ID21942912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88611957..88613467hg38UCSC Ensembl
chr11:88345125..88346635hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg381511
hg191511
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584103
Samples
Known GenesGRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033569
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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