A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1860n100



Internal ID22787947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27834477..28195359hg38UCSC Ensembl
chr14:28303683..28664565hg19UCSC Ensembl
chr14:27373523..27734316hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38360883
hg19360883
hg18360794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039071, nsv1044278
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)dgv1860n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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