A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542156



Internal ID20915420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63354471..63364121hg38UCSC Ensembl
chr20:61985823..61995473hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg389651
hg199651
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203435
Samples
Known GenesCHRNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542156
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