A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861109



Internal ID22636044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65127846..65138731hg38UCSC Ensembl
chr15:65420184..65431069hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3810886
hg1910886
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471751
Samples
Known GenesPDCD7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861109
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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