A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2542n100



Internal ID19012910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32166460..32507614hg38UCSC Ensembl
chr15:32458661..32799815hg19UCSC Ensembl
chr15:30245953..30587107hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38341155
hg19341155
hg18341155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051891, nsv1035203
Samples
Known GenesCHRNA7, GOLGA8K, 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)dgv2542n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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