A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2504n100



Internal ID19012872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30152061..30658787hg38UCSC Ensembl
chr15:30444264..30950990hg19UCSC Ensembl
chr15:28231556..28738282hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38506727
hg19506727
hg18506727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049370, nsv1039255, nsv1049364, nsv1045682, nsv1036109, nsv1050787, nsv1041459, nsv1046268, nsv1054710
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, LOC100288637, LOC101059918, ULK4P1, ULK4P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2504n100
Frequency
Sample Size29084
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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