A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7183n100



Internal ID22793270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40324425..40338108hg38UCSC Ensembl
chr8:40181944..40195627hg19UCSC Ensembl
chr8:40301101..40314784hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3813684
hg1913684
hg1813684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017377, nsv1031415, nsv1030285, nsv1020746, nsv1026582, nsv1033126
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)dgv7183n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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