A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7464n100



Internal ID22793551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16940392..16982737hg38UCSC Ensembl
chr9:16940390..16982735hg19UCSC Ensembl
chr9:16930390..16972735hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3842346
hg1942346
hg1842346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028681, nsv1020828
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)dgv7464n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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