A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520659



Internal ID20894020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39690598..39696393hg38UCSC Ensembl
chr19:40181238..40187033hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg385796
hg195796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047893
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520659
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer