A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077060



Internal ID21986293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81350710..81350710hg38UCSC Ensembl
chr8:82262945..82262945hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077060
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer