A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556170



Internal ID16343579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:103135740..103222216hg38UCSC Ensembl
Innerchr11:103006469..103092945hg19UCSC Ensembl
Innerchr11:102511679..102598155hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3886477
hg1986477
hg1886477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv782100
Samples
Known GenesDYNC2H1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556170
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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