A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv855288



Internal ID16149244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28598169..28609431hg38UCSC Ensembl
Innerchr16:28609490..28620752hg19UCSC Ensembl
Innerchr16:28516991..28528253hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3811263
hg1911263
hg1811263
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571750
Supporting Variants
Samples
Known GenesSULT1A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv855288
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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