A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv411n223



Internal ID22803379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161517901..161540000hg38UCSC Ensembl
chr1:161487691..161509790hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3822100
hg1922100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6329478, nsv6321491
Samples
Known GenesFCGR2A, HSPA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv411n223
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