A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367672



Internal ID21025225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44013797..44027009hg38UCSC Ensembl
chr3:44055289..44068501hg19UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg3813213
hg1913213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367672
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