A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5145n100



Internal ID20156761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15761347..15834614hg38UCSC Ensembl
chr4:15762970..15836237hg19UCSC Ensembl
chr4:15372068..15445335hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3873268
hg1973268
hg1873268
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010597, nsv1013204
Samples
Known GenesCD38
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5145n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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