A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv855242



Internal ID15802512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:27329738..27339704hg38UCSC Ensembl
Innerchr16:27341059..27351025hg19UCSC Ensembl
Innerchr16:27248560..27258526hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg389967
hg199967
hg189967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571718
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)nssv855242
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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