A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556381



Internal ID15997104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107773570..107813645hg38UCSC Ensembl
Innerchr11:107644296..107684371hg19UCSC Ensembl
Innerchr11:107149506..107189581hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3840076
hg1940076
hg1840076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2175n54
Supporting Variantsnssv784215
Samples
Known GenesSLC35F2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556381
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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