A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7459n100



Internal ID22793546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13861067..13923674hg38UCSC Ensembl
chr9:13861066..13923673hg19UCSC Ensembl
chr9:13851066..13913673hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3862608
hg1962608
hg1862608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032113, nsv1032447
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)dgv7459n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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