A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520341



Internal ID20893702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10883935..11045237hg38UCSC Ensembl
chr19:10994611..11155913hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38161303
hg19161303
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198049
Samples
Known GenesC19orf52, CARM1, SMARCA4, YIPF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520341
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