A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008806



Internal ID19098024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161527110..161648229hg38UCSC Ensembl
Innerchr1:161496900..161618019hg19UCSC Ensembl
Innerchr1:159763524..159884643hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38121120
hg19121120
hg18121120
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv449n100
Supporting Variantsnssv3704749, nssv3704748
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)nsv1008806
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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