A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2281n100



Internal ID19012649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20512131..22100273hg38UCSC Ensembl
chr15:20717374..22388224hg19UCSC Ensembl
chr15:18977388..19889588hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381588143
hg191670851
hg18912201
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037599, nsv1039503, nsv1050659, nsv1038182, nsv1036944, nsv1050058, nsv1038139, nsv1042817, nsv1053135, nsv1047453, nsv1054662, nsv1046686, nsv1051392, nsv1047122
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)dgv2281n100
Frequency
Sample Size29084
Observed Gain25
Observed Loss42
Observed Complex0
Frequencyn/a


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