A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv783771



Internal ID16077727
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 loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556298
Supporting Variants
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv783771
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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