A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7137n100



Internal ID19017505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22452539..22546143hg38UCSC Ensembl
chr8:22310052..22403656hg19UCSC Ensembl
chr8:22365997..22459601hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3893605
hg1993605
hg1893605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031436, nsv1033436
Samples
Known GenesPPP3CC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7137n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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