A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1952n100



Internal ID22788039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86898210..86934380hg38UCSC Ensembl
chr14:87364554..87400724hg19UCSC Ensembl
chr14:86434307..86470477hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3836171
hg1936171
hg1836171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045738, nsv1053028
Samples
Known GenesLOC283585
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1952n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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