A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888786



Internal ID22663796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140949661..140949792hg38UCSC Ensembl
chr3:140668503..140668634hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397204
Samples
Known GenesSLC25A36
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888786
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