A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1558n100



Internal ID22787645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:114133855..114197011hg38UCSC Ensembl
chr12:114571660..114634816hg19UCSC Ensembl
chr12:113056043..113119199hg18UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3863157
hg1963157
hg1863157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038223, nsv1053578
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)dgv1558n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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