A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616464



Internal ID21564769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:58315715..58315715hg38UCSC Ensembl
chr2:58542850..58542850hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17114546
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616464
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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