A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv401n223



Internal ID22803369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161501101..161596400hg38UCSC Ensembl
chr1:161470891..161566190hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3895300
hg1995300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6333273, nsv6317700, nsv6329747, nsv6334058, nsv6317121
Samples
Known GenesFCGR2A, FCGR2C, FCGR3A, HSPA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv401n223
Frequency
Sample Size19652
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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