A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556173



Internal ID16343582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:103173309..103301305hg38UCSC Ensembl
Innerchr11:103044038..103172034hg19UCSC Ensembl
Innerchr11:102549248..102677244hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38127997
hg19127997
hg18127997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2140n54
Supporting Variantsnssv782103
Samples
Known GenesDYNC2H1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556173
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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