A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615453



Internal ID21563758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190014433..190014433hg38UCSC Ensembl
chr3:189732222..189732222hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127474
SamplesHG01596
Known GenesLEPREL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615453
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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