A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004196



Internal ID21913539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34369809..34372015hg38UCSC Ensembl
chr6:34337586..34339792hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg382207
hg192207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558521
Samples
Known GenesNUDT3, RPS10-NUDT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004196
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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