A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7136n100



Internal ID19017504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22442859..22542059hg38UCSC Ensembl
chr8:22300372..22399572hg19UCSC Ensembl
chr8:22356317..22455517hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3899201
hg1999201
hg1899201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028675, nsv1017586, nsv1017994
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)dgv7136n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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