A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv855239



Internal ID15802509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:27329738..27337963hg38UCSC Ensembl
Innerchr16:27341059..27349284hg19UCSC Ensembl
Innerchr16:27248560..27256785hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg388226
hg198226
hg188226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571716
Supporting Variants
Samples
Known GenesIL4R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv855239
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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