A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994549



Internal ID21903892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9802431..9802549hg38UCSC Ensembl
chr3:9844115..9844233hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535494
Samples
Known GenesARPC4, ARPC4-TTLL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994549
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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