A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013109



Internal ID18755640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161527110..161678819hg38UCSC Ensembl
Innerchr1:161496900..161648609hg19UCSC Ensembl
Innerchr1:159763524..159915233hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38151710
hg19151710
hg18151710
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv447n100
Supporting Variantsnssv3494109
Samples
Known GenesFCGR2B, FCGR2C, 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)nsv1013109
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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