A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611952



Internal ID21560257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33542681..33542681hg38UCSC Ensembl
chr2:33767748..33767748hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17112975
SamplesHG02011
Known GenesRASGRP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611952
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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