A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068606



Internal ID21977839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184861974..184861974hg38UCSC Ensembl
chr3:184579762..184579762hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555567
Samples
Known GenesVPS8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068606
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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