A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1797n100



Internal ID22787884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20218848..20275110hg38UCSC Ensembl
chr14:20687007..20743269hg19UCSC Ensembl
chr14:19756847..19813109hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3856263
hg1956263
hg1856263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055102, nsv1052883
Samples
Known GenesOR11H4, OR11H6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1797n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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