A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053803



Internal ID19143022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105578021..105733027hg38UCSC Ensembl
Innerchr14:106044358..106199364hg19UCSC Ensembl
Innerchr14:105115403..105270409hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38155007
hg19155007
hg18155007
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1983n100
Supporting Variantsnssv3529834, nssv3529835
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)nsv1053803
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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