A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047601



Internal ID21956835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44801280..44801347hg38UCSC Ensembl
chr19:45304537..45304604hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620697
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047601
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