A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057879



Internal ID19147098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:79367419..79440229hg38UCSC Ensembl
Innerchr17:77363501..77436311hg19UCSC Ensembl
Innerchr17:74875096..74947906hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3872811
hg1972811
hg1872811
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3289n100
Supporting Variantsnssv3567857
Samples
Known GenesRBFOX3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057879
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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