A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526318



Internal ID20899679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40745861..40746566hg38UCSC Ensembl
chr19:41251766..41252471hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047771
Samples
Known GenesC19orf54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526318
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