A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610882



Internal ID21559187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:33631111..33631111hg38UCSC Ensembl
chr4:33632733..33632733hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121839
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610882
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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