A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614184



Internal ID21562489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167922751..167922751hg38UCSC Ensembl
chr2:168779261..168779261hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110535
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614184
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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