A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571716



Internal ID16012439
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 StatusM
Merged Variantsdgv4963n54
Supporting Variantsnssv855238, nssv855239
Samples
Known GenesIL4R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571716
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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