A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660335



Internal ID21608640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134408189..134408189hg38UCSC Ensembl
chr11:134278083..134278083hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073181
SamplesHG03125
Known GenesB3GAT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660335
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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