A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368482



Internal ID21026035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47902891..47923337hg38UCSC Ensembl
chr3:47944381..47964827hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3820447
hg1920447
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209320
Samples
Known GenesMAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368482
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