A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556226



Internal ID16343635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106527293..106528755hg38UCSC Ensembl
Innerchr11:106398020..106399482hg19UCSC Ensembl
Innerchr11:105903230..105904692hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381463
hg191463
hg181463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175397
SamplesHGDP00618
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556226
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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