A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1859n100



Internal ID22787946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27438530..27555238hg38UCSC Ensembl
chr14:27907736..28024444hg19UCSC Ensembl
chr14:26977576..27094284hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38116709
hg19116709
hg18116709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045076, nsv1040926, nsv1039343
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)dgv1859n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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