A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007142



Internal ID21916485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127740015..127745884hg38UCSC Ensembl
chr8:128752261..128758130hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg385870
hg195870
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582598
Samples
Known GenesMYC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007142
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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