A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060183



Internal ID21969416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38603353..38603419hg38UCSC Ensembl
chr19:39093993..39094059hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626167
Samples
Known GenesMAP4K1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060183
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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