A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619678



Internal ID21567983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37163862..37163862hg38UCSC Ensembl
chr3:37205353..37205353hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124975
SamplesHG01114
Known GenesLRRFIP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619678
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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