A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3529822



Internal ID18481417
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 StatusS
Merged Variantsnsv1054302
Supporting Variants
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)nssv3529822
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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