A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613256



Internal ID21561561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98838444..98838444hg38UCSC Ensembl
chr3:98557288..98557288hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132441
SamplesNA19238
Known GenesDCBLD2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613256
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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