A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852311



Internal ID15799581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4315234..4338138hg38UCSC Ensembl
Innerchr16:4365235..4388139hg19UCSC Ensembl
Innerchr16:4305236..4328140hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3822905
hg1922905
hg1822905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571282
Supporting Variants
Samples
Known GenesGLIS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852311
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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