A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713383



Internal ID19011664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18559262..19265122hg38UCSC Ensembl
Innerchr14:19335739..19852821hg19UCSC Ensembl
Innerchr14:18405739..18922821hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38705861
hg19517083
hg18517083
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053750
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)nssv3713383
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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