A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361471



Internal ID21019024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:168606153..168630599hg38UCSC Ensembl
chr3:168323941..168348387hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3824447
hg1924447
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209188
Samples
Known GenesEGFEM1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361471
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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