A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615475



Internal ID21563780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13450018..13450018hg38UCSC Ensembl
chr3:13491518..13491518hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125914, nssv17119965
SamplesNA19238, NA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615475
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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