A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567285



Internal ID21515619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:898797..898994hg38UCSC Ensembl
chr5:898912..899109hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151618
SamplesHG03065
Known GenesTRIP13
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567285
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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