A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2546n100



Internal ID19012914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32247324..32507614hg38UCSC Ensembl
chr15:32539525..32799815hg19UCSC Ensembl
chr15:30326817..30587107hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38260291
hg19260291
hg18260291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049585, nsv1049139, nsv1048737, nsv1040206
Samples
Known GenesGOLGA8K, GOLGA8O, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2546n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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