A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433903



Internal ID21395905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148390809..148391337hg38UCSC Ensembl
chr3:148108596..148109124hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv530n172
Supporting Variantsnssv15749555
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433903
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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