A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2266n100



Internal ID22788353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20372247..20625059hg38UCSC Ensembl
chr15:20577500..20830362hg19UCSC Ensembl
chr15:18837514..19090376hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38252813
hg19252863
hg18252863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040174, nsv1043896, nsv1047018, nsv1044557, nsv1054217, nsv1044133, nsv1046187, nsv1039317, nsv1049358, nsv1051339
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2266n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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