A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1751n100



Internal ID20153367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:18225635..19289336hg38UCSC Ensembl
chr14:19002112..19877060hg19UCSC Ensembl
chr14:18072112..18947060hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381063702
hg19874949
hg18874949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045932, nsv1035372
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)dgv1751n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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