A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556298



Internal ID16343707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107368380..107371425hg38UCSC Ensembl
Innerchr11:107239106..107242151hg19UCSC Ensembl
Innerchr11:106744316..106747361hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg383046
hg193046
hg183046
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv783772, nssv783773, nssv783771, nssv783770
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556298
Frequency
Sample Size17421
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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