A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2654n100



Internal ID22788741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87266138..87327490hg38UCSC Ensembl
chr15:87809369..87870721hg19UCSC Ensembl
chr15:85610373..85671725hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3861353
hg1961353
hg1861353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038769, nsv1043845
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)dgv2654n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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