A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552998



Internal ID16340407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1561057..1568925hg38UCSC Ensembl
Innerchr11:1582287..1590155hg19UCSC Ensembl
Innerchr11:1538863..1546731hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg387869
hg197869
hg187869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1553n54
Supporting Variantsnssv764303
Samples
Known GenesDUSP8, MOB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552998
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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