A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613378



Internal ID21561683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16009083..16009083hg38UCSC Ensembl
chr2:16149205..16149205hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109413
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613378
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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