A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578687



Internal ID21527159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15062198..15062505hg38UCSC Ensembl
chr3:15103705..15104012hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122583
SamplesNA19239
Known GenesMRPS25
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578687
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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