A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571721



Internal ID16012444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:27335033..27339704hg38UCSC Ensembl
Innerchr16:27346354..27351025hg19UCSC Ensembl
Innerchr16:27253855..27258526hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg384672
hg194672
hg184672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv855249
Samples
Known GenesIL4R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571721
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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