A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2552n100



Internal ID19012920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34376855..34750571hg38UCSC Ensembl
chr15:34669056..35042772hg19UCSC Ensembl
chr15:32456348..32830064hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38373717
hg19373717
hg18373717
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054985, nsv1040900
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2, MIR5588
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2552n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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