A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556384



Internal ID15997107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107780369..107801319hg38UCSC Ensembl
Innerchr11:107651095..107672045hg19UCSC Ensembl
Innerchr11:107156305..107177255hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3820951
hg1920951
hg1820951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2176n54
Supporting Variantsnssv784219
Samples
Known GenesSLC35F2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556384
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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