A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943966



Internal ID22719423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12958739..12958897hg38UCSC Ensembl
chr19:13069553..13069711hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943966
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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