A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036979



Internal ID19126198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104597521..104607743hg38UCSC Ensembl
Innerchr9:107359802..107370024hg19UCSC Ensembl
Innerchr9:106399623..106409845hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3810223
hg1910223
hg1810223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7696n100
Supporting Variantsnssv3697634
Samples
Known GenesOR13C2, OR13C5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036979
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