A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713340



Internal ID18664935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..19119026hg38UCSC Ensembl
Innerchr14:19002112..19706746hg19UCSC Ensembl
Innerchr14:18072112..18776746hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38893392
hg19704635
hg18704635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036376
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, POTEG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713340
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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