A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618923



Internal ID21567228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122414100..122414100hg38UCSC Ensembl
chr3:122132947..122132947hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120310
SamplesNA20847
Known GenesWDR5B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618923
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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