A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043870



Internal ID21953161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51322341..51322439hg38UCSC Ensembl
chr19:51825595..51825693hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619977
Samples
Known GenesIGLON5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043870
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