A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615474



Internal ID21563779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149087159..149087159hg38UCSC Ensembl
chr1:148351790..148351790hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060593
SamplesNA19239
Known GenesLOC101929780
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615474
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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