A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1559n100



Internal ID22787646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:115722735..115735997hg38UCSC Ensembl
chr12:116160540..116173802hg19UCSC Ensembl
chr12:114644923..114658185hg18UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3813263
hg1913263
hg1813263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052372, nsv1044139, nsv1050492
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)dgv1559n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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