A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791927



Internal ID19162467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18580235..19763052hg38UCSC Ensembl
Innerchr14:19356712..20231211hg19UCSC Ensembl
Innerchr14:18426712..19301051hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381182818
hg19874500
hg18874340
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892461
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, OR11H2, OR4Q3, POTEG, POTEM
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=115
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791927
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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