A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7482n100



Internal ID22793569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:24930303..25019895hg38UCSC Ensembl
chr9:24930301..25019893hg19UCSC Ensembl
chr9:24920301..25009893hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3889593
hg1989593
hg1889593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017523, nsv1031065
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)dgv7482n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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