A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616443



Internal ID21564748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27315580..27315580hg38UCSC Ensembl
chr3:27357071..27357071hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121716
SamplesHG02818
Known GenesNEK10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616443
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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