A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1894n100



Internal ID22787981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:43761908..44437311hg38UCSC Ensembl
chr14:44231111..44906514hg19UCSC Ensembl
chr14:43300861..43976264hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38675404
hg19675404
hg18675404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038633, nsv1047006
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)dgv1894n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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