A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2280n100



Internal ID19012648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20512131..22098952hg38UCSC Ensembl
chr15:20717374..22386903hg19UCSC Ensembl
chr15:18977388..19888267hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381586822
hg191669530
hg18910880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041256, nsv1053746, nsv1039490, nsv1042564, nsv1045938, nsv1042592
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N4, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2280n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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