A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045227



Internal ID21954497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39455769..39455879hg38UCSC Ensembl
chr19:39946409..39946519hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633074
Samples
Known GenesSUPT5H
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045227
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