A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3490643



Internal ID18731598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161543969..161690238hg38UCSC Ensembl
Innerchr1:161513759..161660028hg19UCSC Ensembl
Innerchr1:159780383..159926652hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38146270
hg19146270
hg18146270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005425
Supporting Variants
Samples
Known GenesFCGR2B, FCGR2C, FCGR3A, FCGR3B, HSPA7, RPL31P11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3490643
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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