A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051819



Internal ID19141038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105544959..105728426hg38UCSC Ensembl
Innerchr14:106011296..106194763hg19UCSC Ensembl
Innerchr14:105082341..105265808hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38183468
hg19183468
hg18183468
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1983n100
Supporting Variantsnssv3529823
Samples
Known GenesELK2AP, MIR8071-1, MIR8071-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051819
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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