A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14248010



Internal ID21313114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:80689879..80879791hg38UCSC Ensembl
Outerchr3:80683567..80884445hg38UCSC Ensembl
Innerchr3:80739030..80928942hg19UCSC Ensembl
Outerchr3:80732718..80933596hg19UCSC Ensembl
Innerchr3:80821720..81011632hg18UCSC Ensembl
Outerchr3:80815408..81016286hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38200879
hg19200879
hg18200879
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170313
Supporting Variants
SamplesSNI_7
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14248010
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