A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434193



Internal ID21091746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101204801..101207100hg38UCSC Ensembl
chr8:102217029..102219328hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217647
Samples
Known GenesZNF706
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434193
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