A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169664



Internal ID21313475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94389494..94395812hg38UCSC Ensembl
Outerchr14:94387628..94397299hg38UCSC Ensembl
Innerchr14:94855831..94862149hg19UCSC Ensembl
Outerchr14:94853965..94863636hg19UCSC Ensembl
Innerchr14:93925584..93931902hg18UCSC Ensembl
Outerchr14:93923718..93933389hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg389672
hg199672
hg189672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242747
SamplesNGO_14
Known GenesSERPINA1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169664
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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