A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411335



Internal ID22469205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:79125898..79125972hg38UCSC Ensembl
chr3:79175048..79175122hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894434
Supporting Variants
Samples
Known GenesROBO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411335
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