A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069014



Internal ID21978247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126143341..126143341hg38UCSC Ensembl
chr8:127155585..127155585hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585841
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069014
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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