A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169786



Internal ID21313597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42425537..42483682hg38UCSC Ensembl
Outerchr14:42424146..42489042hg38UCSC Ensembl
Innerchr14:42894740..42952885hg19UCSC Ensembl
Outerchr14:42893349..42958245hg19UCSC Ensembl
Innerchr14:41964490..42022635hg18UCSC Ensembl
Outerchr14:41963099..42027995hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3864897
hg1964897
hg1864897
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14243999
SamplesNGO_28
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169786
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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