A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866446



Internal ID16160402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3287239..3318238hg38UCSC Ensembl
Innerchr17:3190533..3221532hg19UCSC Ensembl
Innerchr17:3137283..3168282hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3831000
hg1931000
hg1831000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574235
Supporting Variants
Samples
Known GenesOR3A1, OR3A4P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866446
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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