A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2572n100



Internal ID20154188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34464686..34565797hg38UCSC Ensembl
chr15:34756887..34857998hg19UCSC Ensembl
chr15:32544179..32645290hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38101112
hg19101112
hg18101112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035584, nsv1039827
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2572n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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