A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7381n100



Internal ID22793468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4903296..4948105hg38UCSC Ensembl
chr9:4903296..4948105hg19UCSC Ensembl
chr9:4893296..4938105hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3844810
hg1944810
hg1844810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030568, nsv1032013
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)dgv7381n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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