A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7469n100



Internal ID22793556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18270457..18299448hg38UCSC Ensembl
chr9:18270455..18299446hg19UCSC Ensembl
chr9:18260455..18289446hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3828992
hg1928992
hg1828992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015972, nsv1020662
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)dgv7469n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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