A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613458



Internal ID21561763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84029615..84029615hg38UCSC Ensembl
chr4:84950768..84950768hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119706
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613458
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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