A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263512



Internal ID20472730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:79125895..79125968hg38UCSC Ensembl
chr3:79175045..79175118hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731640
Supporting Variants
Samples
Known GenesROBO1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263512
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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