A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6180n223



Internal ID22809148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49460301..49484400hg38UCSC Ensembl
chr6:49428014..49452113hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3824100
hg1924100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6410099, nsv6411952
Samples
Known GenesCENPQ, MUT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6180n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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