A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2526n100



Internal ID19012894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30438488..30818328hg38UCSC Ensembl
chr15:30730691..31110531hg19UCSC Ensembl
chr15:28517983..28897823hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38379841
hg19379841
hg18379841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054207, nsv1052035, nsv1039169, nsv1035820, nsv1054817, nsv1039757, nsv1044767, nsv1046246, nsv1051269, nsv1039869
Samples
Known GenesARHGAP11B, GOLGA8H, HERC2P10, LOC100288637, ULK4P1, ULK4P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2526n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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