A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047327



Internal ID19136546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18661498..19922383hg38UCSC Ensembl
Innerchr14:19437975..20390542hg19UCSC Ensembl
Innerchr14:18507975..19460382hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381260886
hg19952568
hg18952408
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1759n100
Supporting Variantsnssv3528007
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3, POTEG, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047327
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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