A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7124n100



Internal ID22793211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18094228..18136829hg38UCSC Ensembl
chr8:17951737..17994338hg19UCSC Ensembl
chr8:17996017..18038618hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3842602
hg1942602
hg1842602
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027839, nsv1021307, nsv1024294, nsv1029126
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)dgv7124n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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