A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169419



Internal ID21313902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:33186351..33209038hg38UCSC Ensembl
Outerchr14:33182689..33209922hg38UCSC Ensembl
Innerchr14:33655557..33678244hg19UCSC Ensembl
Outerchr14:33651895..33679128hg19UCSC Ensembl
Innerchr14:32725308..32747995hg18UCSC Ensembl
Outerchr14:32721646..32748879hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3827234
hg1927234
hg1827234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14243459, nssv14250607
SamplesNGO_14, NGO_26
Known GenesNPAS3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169419
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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