A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855342



Internal ID22630277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62080072..62093325hg38UCSC Ensembl
chr15:62372271..62385524hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3813254
hg1913254
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472976
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855342
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