A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571717



Internal ID16012440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:27329738..27339366hg38UCSC Ensembl
Innerchr16:27341059..27350687hg19UCSC Ensembl
Innerchr16:27248560..27258188hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg389629
hg199629
hg189629
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4963n54
Supporting Variantsnssv855240
Samples
Known GenesIL4R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571717
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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