A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556176



Internal ID16343585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:103257781..103408370hg38UCSC Ensembl
Innerchr11:103128510..103279098hg19UCSC Ensembl
Innerchr11:102633720..102784308hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38150590
hg19150589
hg18150589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2141n54
Supporting Variantsnssv782106
Samples
Known GenesDYNC2H1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556176
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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