A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1507n54



Internal ID20134931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:368778..382912hg38UCSC Ensembl
chr11:368778..382912hg19UCSC Ensembl
chr11:358778..372912hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3814135
hg1914135
hg1814135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552778, nsv552777
Samples
Known GenesB4GALNT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1507n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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