A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1858n100



Internal ID22787945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27287258..27374103hg38UCSC Ensembl
chr14:27756464..27843309hg19UCSC Ensembl
chr14:26826304..26913149hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3886846
hg1986846
hg1886846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038085, nsv1041455, nsv1045407
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)dgv1858n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer