A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1803n100



Internal ID20153419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21959708..22509792hg38UCSC Ensembl
chr14:22427926..22978775hg19UCSC Ensembl
chr14:21497766..22048615hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38550085
hg19550850
hg18550850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054356, nsv1036409, nsv1036343, nsv1049135, nsv1045117
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)dgv1803n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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