A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526946



Internal ID18825227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18559262..19256386hg38UCSC Ensembl
Innerchr14:19335739..19844095hg19UCSC Ensembl
Innerchr14:18405739..18914095hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38697125
hg19508357
hg18508357
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043334
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)nssv3526946
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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