A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866444



Internal ID16160400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3208286..3290664hg38UCSC Ensembl
Innerchr17:3111580..3193958hg19UCSC Ensembl
Innerchr17:3058330..3140708hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3882379
hg1982379
hg1882379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574231
Supporting Variants
Samples
Known GenesOR1A1, OR1D4, OR3A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866444
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer