A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7426n100



Internal ID22793513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11868796..12398327hg38UCSC Ensembl
chr9:11868796..12398327hg19UCSC Ensembl
chr9:11858796..12388327hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38529532
hg19529532
hg18529532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016898, nsv1032107, nsv1029232, nsv1028253
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)dgv7426n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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