A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556388



Internal ID15997111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107785223..107802574hg38UCSC Ensembl
Innerchr11:107655949..107673300hg19UCSC Ensembl
Innerchr11:107161159..107178510hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3817352
hg1917352
hg1817352
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2176n54
Supporting Variantsnssv784269, nssv784271, nssv784270
Samples
Known GenesSLC35F2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556388
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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