A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555633



Internal ID16343042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85715287..85762840hg38UCSC Ensembl
Innerchr11:85426330..85473883hg19UCSC Ensembl
Innerchr11:85103978..85151531hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3847554
hg1947554
hg1847554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2040n54
Supporting Variantsnssv779873
Samples
Known GenesSYTL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555633
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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