A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169838



Internal ID21313649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:28105450..28140816hg38UCSC Ensembl
Outerchr3:28102355..28142764hg38UCSC Ensembl
Innerchr3:28146941..28182307hg19UCSC Ensembl
Outerchr3:28143846..28184255hg19UCSC Ensembl
Innerchr3:28121945..28157311hg18UCSC Ensembl
Outerchr3:28118850..28159259hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3840410
hg1940410
hg1840410
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14241521
SamplesNGO_22
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169838
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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