A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054126



Internal ID19143345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20964296..20987933hg38UCSC Ensembl
Innerchr14:21432455..21456092hg19UCSC Ensembl
Innerchr14:20502295..20525932hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3823638
hg1923638
hg1823638
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532167
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054126
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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