A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556379



Internal ID16343788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107756883..107800900hg38UCSC Ensembl
Innerchr11:107627609..107671626hg19UCSC Ensembl
Innerchr11:107132819..107176836hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3844018
hg1944018
hg1844018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2174n54
Supporting Variantsnssv784210, nssv784209, nssv784211
Samples
Known GenesSLC35F2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556379
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer