A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430148



Internal ID21087701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21583435..21586876hg38UCSC Ensembl
chr8:21440946..21444387hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg383442
hg193442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166082
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430148
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