A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609427



Internal ID21557732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42497115..42497115hg38UCSC Ensembl
chr3:42538607..42538607hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126764
SamplesHG02587
Known GenesVIPR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609427
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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