A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429173



Internal ID21086726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19908301..19911600hg38UCSC Ensembl
chr8:19765812..19769111hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7294n223
Supporting Variantsnssv18227803
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429173
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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