A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555239



Internal ID16342648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67028909..67049036hg38UCSC Ensembl
Innerchr11:66796380..66816507hg19UCSC Ensembl
Innerchr11:66552956..66573083hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3820128
hg1920128
hg1820128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1973n54
Supporting Variantsnssv778548
Samples
Known GenesMIR6860, SYT12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555239
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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