A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932649



Internal ID22707951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59488719..59489007hg38UCSC Ensembl
chr15:59780918..59781206hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387903
Samples
Known GenesFAM81A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932649
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