A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852532



Internal ID15799802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11953042..11968539hg38UCSC Ensembl
Innerchr16:12046899..12062396hg19UCSC Ensembl
Innerchr16:11954400..11969897hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3815498
hg1915498
hg1815498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571459
Supporting Variants
Samples
Known GenesTNFRSF17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852532
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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