A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520984



Internal ID20894345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40773636..40774538hg38UCSC Ensembl
chr19:41279541..41280443hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38903
hg19903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047772
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520984
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