A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1805n100



Internal ID22787892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22107259..22509792hg38UCSC Ensembl
chr14:22575536..22978775hg19UCSC Ensembl
chr14:21645376..22048615hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38402534
hg19403240
hg18403240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041224, nsv1036750, nsv1035178, nsv1045789, nsv1053889, nsv1043500, nsv1053932, nsv1037675, nsv1049042, nsv1048771, nsv1043285, nsv1050899, nsv1052166, nsv1037474, nsv1048895, nsv1038976, nsv1051461, nsv1050861, nsv1049882
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1805n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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