A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609190



Internal ID21557495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45651000..45651000hg38UCSC Ensembl
chr3:45692492..45692492hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131394
SamplesHG00731
Known GenesLIMD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609190
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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