A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2551n100



Internal ID19012919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34376855..34454249hg38UCSC Ensembl
chr15:34669056..34746450hg19UCSC Ensembl
chr15:32456348..32533742hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3877395
hg1977395
hg1877395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050702, nsv1048913
Samples
Known GenesGOLGA8A, 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)dgv2551n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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