A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2675n100



Internal ID20154291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101395007..101771043hg38UCSC Ensembl
chr15:101935212..102311246hg19UCSC Ensembl
chr15:99752735..100128769hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38376037
hg19376035
hg18376035
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052550, nsv1039393, nsv1036892, nsv1046105, nsv1038835
Samples
Known GenesPCSK6, TARSL2, TM2D3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2675n100
Frequency
Sample Size29084
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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