A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14252012



Internal ID21304333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84234018..84267664hg38UCSC Ensembl
Outerchr3:84230625..84278110hg38UCSC Ensembl
Innerchr3:84283169..84316815hg19UCSC Ensembl
Outerchr3:84279776..84327261hg19UCSC Ensembl
Innerchr3:84365859..84399505hg18UCSC Ensembl
Outerchr3:84362466..84409951hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3847486
hg1947486
hg1847486
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169964
Supporting Variants
SamplesNGO_12
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14252012
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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