A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063339



Internal ID21972572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1298092..1298092hg38UCSC Ensembl
chr8:1246351..1246351hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563428
Samples
Known GenesLOC286083
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063339
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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