A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620671



Internal ID21568976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167684952..167684952hg38UCSC Ensembl
chr3:167402740..167402740hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132547
SamplesHG00864
Known GenesPDCD10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620671
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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