A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1552n54



Internal ID22769447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1510132..1512743hg38UCSC Ensembl
chr11:1531362..1533973hg19UCSC Ensembl
chr11:1487938..1490549hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382612
hg192612
hg182612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552993, nsv552995
Samples
Known GenesMOB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1552n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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