A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036562



Internal ID18779093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105521689..105989851hg38UCSC Ensembl
Innerchr14:105988026..106455941hg19UCSC Ensembl
Innerchr14:105059071..105526986hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38468163
hg19467916
hg18467916
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1982n100
Supporting Variantsnssv3711395
Samples
Known GenesADAM6, ELK2AP, KIAA0125, MIR8071-1, MIR8071-2, TMEM121
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036562
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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