A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938862



Internal ID22714248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72609762..72609845hg38UCSC Ensembl
chr15:72902103..72902186hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374620
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938862
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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