A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019871



Internal ID21929214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89994564..89994618hg38UCSC Ensembl
chr8:91006792..91006846hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584063
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019871
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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