A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007080



Internal ID19096298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161527110..161648747hg38UCSC Ensembl
Innerchr1:161496900..161618537hg19UCSC Ensembl
Innerchr1:159763524..159885161hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38121638
hg19121638
hg18121638
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv449n100
Supporting Variantsnssv3488764, nssv3493302
Samples
Known GenesFCGR2C, FCGR3A, FCGR3B, HSPA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007080
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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