A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587141



Internal ID21535701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35296788..35296946hg38UCSC Ensembl
chr15:35588989..35589147hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096683
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587141
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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