A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524356



Internal ID20897717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1896306..1946570hg38UCSC Ensembl
chr19:1896305..1946569hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3850265
hg1950265
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198361
Samples
Known GenesADAT3, CSNK1G2, SCAMP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524356
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