A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054302



Internal ID18796833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105521689..105659049hg38UCSC Ensembl
Innerchr14:105988026..106125386hg19UCSC Ensembl
Innerchr14:105059071..105196431hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38137361
hg19137361
hg18137361
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1981n100
Supporting Variantsnssv3529822
Samples
Known GenesMIR8071-1, 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)nsv1054302
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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