A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934517



Internal ID22709845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40707243..40707552hg38UCSC Ensembl
chr15:40999441..40999750hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381932
Samples
Known GenesRAD51
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934517
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