A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv779883



Internal ID16073839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85745660..85753879hg38UCSC Ensembl
Innerchr11:85456703..85464922hg19UCSC Ensembl
Innerchr11:85134351..85142570hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg388220
hg198220
hg188220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555640
Supporting Variants
Samples
Known GenesSYTL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv779883
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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