A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646334



Internal ID21594639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134408225..134408225hg38UCSC Ensembl
chr11:134278119..134278119hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381476
hg191476
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073585
SamplesHG03125
Known GenesB3GAT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646334
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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