A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530668



Internal ID20904029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4069969..4218383hg38UCSC Ensembl
chr19:4069967..4218380hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38148415
hg19148414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198146
Samples
Known GenesANKRD24, CREB3L3, MAP2K2, SIRT6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530668
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