A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555634



Internal ID16343043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85719354..85753879hg38UCSC Ensembl
Innerchr11:85430397..85464922hg19UCSC Ensembl
Innerchr11:85108045..85142570hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3834526
hg1934526
hg1834526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2040n54
Supporting Variantsnssv779874
Samples
Known GenesSYTL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555634
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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