A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2152n100



Internal ID20153768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106610253..106877229hg38UCSC Ensembl
chr14:107066263..107285437hg19UCSC Ensembl
chr14:106137308..106356482hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38266977
hg19219175
hg18219175
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045990, nsv1049574, nsv1038194
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)dgv2152n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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