A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7460n100



Internal ID22793547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15378194..15416661hg38UCSC Ensembl
chr9:15378192..15416659hg19UCSC Ensembl
chr9:15368192..15406659hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3838468
hg1938468
hg1838468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022227, nsv1032861
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)dgv7460n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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