A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17566133



Internal ID21758176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34303330..34303330hg38UCSC Ensembl
chr6:34271107..34271107hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061935
Supporting Variants
Samples
Known GenesNUDT3, RPS10-NUDT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17566133
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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