A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320378



Internal ID20853476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161550223..161631579hg38UCSC Ensembl
chr1:161520013..161601369hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3881357
hg1981357
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv415n223
Supporting Variantsnssv18201247
Samples
Known GenesFCGR2C, FCGR3A, FCGR3B, HSPA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320378
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