A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7128n100



Internal ID19017496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18994017..19008815hg38UCSC Ensembl
chr8:18851527..18866325hg19UCSC Ensembl
chr8:18895807..18910605hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3814799
hg1914799
hg1814799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1023757, nsv1032307, nsv1024637, nsv1023378
Samples
Known GenesPSD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7128n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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