A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051709



Internal ID21960942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50459458..50459533hg38UCSC Ensembl
chr19:50962715..50962790hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619993
Samples
Known GenesMYBPC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051709
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