A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3442n100



Internal ID19013810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15197257..15238422hg38UCSC Ensembl
chr19:15308068..15349233hg19UCSC Ensembl
chr19:15169068..15210233hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3841166
hg1941166
hg1841166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060266, nsv1066481
Samples
Known GenesBRD4, EPHX3, NOTCH3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3442n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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