A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534973



Internal ID20908334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4839722..4849336hg38UCSC Ensembl
chr19:4839734..4849348hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg389615
hg199615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048384
Samples
Known GenesPLIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534973
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