A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526729



Internal ID20900090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45198534..45207422hg38UCSC Ensembl
chr19:45701792..45710680hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg388889
hg198889
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198873
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526729
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