A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900570



Internal ID22675713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146940880..147108538hg38UCSC Ensembl
chr3:146658667..146826325hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38167659
hg19167659
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429536
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900570
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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