A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366643



Internal ID21024196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32909811..32915224hg38UCSC Ensembl
chr3:32951303..32956716hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg385414
hg195414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4834n223
Supporting Variantsnssv18099430
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366643
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