A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2578n100



Internal ID22788665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38904463..39096681hg38UCSC Ensembl
chr15:39196664..39388882hg19UCSC Ensembl
chr15:36983956..37176174hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38192219
hg19192219
hg18192219
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043614, nsv1051742
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)dgv2578n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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