A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616305



Internal ID21564610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:197361697..197361697hg38UCSC Ensembl
chr2:198226421..198226421hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38784
hg19784
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110980
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616305
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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