A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064116



Internal ID21973349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1298038..1298038hg38UCSC Ensembl
chr8:1246294..1246294hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561835
Samples
Known GenesLOC286083
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064116
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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