A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366589



Internal ID21024142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48534932..48551285hg38UCSC Ensembl
chr3:48572365..48588718hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3816354
hg1916354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101441
Samples
Known GenesMIR6823, PFKFB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366589
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer