A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368922



Internal ID21026475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186786474..186794823hg38UCSC Ensembl
chr3:186504263..186512612hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg388350
hg198350
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212216
Samples
Known GenesEIF4A2, MIR1248, RFC4, SNORA4, SNORA63, SNORA81
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368922
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