A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555831



Internal ID16343240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90118521..90184531hg38UCSC Ensembl
Innerchr11:89851689..89917699hg19UCSC Ensembl
Innerchr11:89491337..89557347hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3866011
hg1966011
hg1866011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv780543
Samples
Known GenesNAALAD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555831
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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