A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345829



Internal ID21003382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:193282403..194049219hg38UCSC Ensembl
chr2:194147128..194913943hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38766817
hg19766816
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205464
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345829
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