A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5605877



Internal ID21554182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189312136..189312136hg38UCSC Ensembl
chr3:189029925..189029925hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125727
SamplesNA19239
Known GenesTPRG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5605877
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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