A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556297



Internal ID16343706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107368380..107371417hg38UCSC Ensembl
Innerchr11:107239106..107242143hg19UCSC Ensembl
Innerchr11:106744316..106747353hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg383038
hg193038
hg183038
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv783769
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556297
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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