A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651838



Internal ID21600143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74682317..74682317hg38UCSC Ensembl
chr15:74974658..74974658hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg382758
hg192758
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080668
SamplesHG00096
Known GenesEDC3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651838
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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