A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2582n100



Internal ID20154198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41791376..41900562hg38UCSC Ensembl
chr15:42083574..42192760hg19UCSC Ensembl
chr15:39870866..39980052hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38109187
hg19109187
hg18109187
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051200, nsv1051733, nsv1038393, nsv1041645, nsv1036153, nsv1048606
Samples
Known GenesEHD4, JMJD7, JMJD7-PLA2G4B, MAPKBP1, MIR4310, PLA2G4B, SPTBN5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2582n100
Frequency
Sample Size29084
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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