A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613630



Internal ID21561935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9113356..9113356hg38UCSC Ensembl
chr2:9253485..9253485hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115434
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613630
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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