A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3941378



Internal ID21361447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77036103..77036103hg38UCSC Ensembl
chr8:77948339..77948339hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204452
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3941378
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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