A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2591n100



Internal ID22788678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45916829..46061687hg38UCSC Ensembl
chr15:46209027..46353885hg19UCSC Ensembl
chr15:43996319..44141177hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38144859
hg19144859
hg18144859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046789, nsv1043776
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)dgv2591n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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