A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945840



Internal ID22721321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33669309..33677156hg38UCSC Ensembl
chr13:34243446..34251293hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg387848
hg197848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388174
Samples
Known GenesSTARD13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945840
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