A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2548n100



Internal ID19012916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32323088..32584771hg38UCSC Ensembl
chr15:32615289..32876972hg19UCSC Ensembl
chr15:30402581..30664264hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38261684
hg19261684
hg18261684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053532, nsv1049704, nsv1042788
Samples
Known GenesGOLGA8K, GOLGA8O, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2548n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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