A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900498



Internal ID22675641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78829532..78830482hg38UCSC Ensembl
chr3:78878682..78879632hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38951
hg19951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421880
Samples
Known GenesROBO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900498
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