A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042504



Internal ID21951820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9382404..9382404hg38UCSC Ensembl
chr3:9424088..9424088hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526786
Samples
Known GenesTHUMPD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042504
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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