A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064377



Internal ID21973610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142932702..142932702hg38UCSC Ensembl
chr3:142651544..142651544hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555005
Samples
Known GenesLOC100507389
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064377
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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