A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv779878



Internal ID16073834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85720843..85754136hg38UCSC Ensembl
Innerchr11:85431886..85465179hg19UCSC Ensembl
Innerchr11:85109534..85142827hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3833294
hg1933294
hg1833294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555636
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)nssv779878
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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