A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852079



Internal ID15799349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1974897..1979722hg38UCSC Ensembl
Innerchr16:2024898..2029723hg19UCSC Ensembl
Innerchr16:1964899..1969724hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg384826
hg194826
hg184826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571186
Supporting Variants
Samples
Known GenesNOXO1, TBL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852079
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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