A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040078



Internal ID19129297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22208199..22481502hg38UCSC Ensembl
Innerchr14:22676095..22950491hg19UCSC Ensembl
Innerchr14:21745935..22020331hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38273304
hg19274397
hg18274397
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1806n100
Supporting Variantsnssv3532248
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)nsv1040078
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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