A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571720



Internal ID16012443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:27329738..27340800hg38UCSC Ensembl
Innerchr16:27341059..27352121hg19UCSC Ensembl
Innerchr16:27248560..27259622hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3811063
hg1911063
hg1811063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4963n54
Supporting Variantsnssv855248, nssv855247
Samples
Known GenesIL4R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571720
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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