A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552993



Internal ID16340402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1510132..1512743hg38UCSC Ensembl
Innerchr11:1531362..1533973hg19UCSC Ensembl
Innerchr11:1487938..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 Variantsdgv1552n54
Supporting Variantsnssv764295, nssv764296, nssv764294
Samples
Known GenesMOB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552993
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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