A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368825



Internal ID21026378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39404823..39420852hg38UCSC Ensembl
chr3:39446314..39462343hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3816030
hg1916030
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211205
Samples
Known GenesRPSA, SNORA6, SNORA62
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368825
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