A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622046



Internal ID21570351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3590500..3590500hg38UCSC Ensembl
chr2:3638090..3638090hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113114
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622046
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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