A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7416n100



Internal ID22793503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11694489..11967982hg38UCSC Ensembl
chr9:11694489..11967982hg19UCSC Ensembl
chr9:11684489..11957982hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38273494
hg19273494
hg18273494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025645, nsv1022308
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)dgv7416n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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