A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330268



Internal ID20863424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161625901..161627300hg38UCSC Ensembl
chr1:161595691..161597090hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201289
Samples
Known GenesFCGR3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330268
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