A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571715



Internal ID16012438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:27329738..27337568hg38UCSC Ensembl
Innerchr16:27341059..27348889hg19UCSC Ensembl
Innerchr16:27248560..27256390hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg387831
hg197831
hg187831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4963n54
Supporting Variantsnssv855237
Samples
Known GenesIL4R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571715
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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