A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900107



Internal ID22675246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190856222..190856287hg38UCSC Ensembl
chr3:190574011..190574076hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417210
Samples
Known GenesGMNC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900107
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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