A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941459



Internal ID22716883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57282595..57286152hg38UCSC Ensembl
chr15:57574793..57578350hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg383558
hg193558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377431
Samples
Known GenesTCF12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941459
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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