A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2671n100



Internal ID22788758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101121007..101153676hg38UCSC Ensembl
chr15:101661212..101693881hg19UCSC Ensembl
chr15:99478735..99511404hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3832670
hg1932670
hg1832670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053546, nsv1036288
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)dgv2671n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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