A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011277



Internal ID18753811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161553748..161652367hg38UCSC Ensembl
Innerchr1:161523538..161622157hg19UCSC Ensembl
Innerchr1:159790162..159888781hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3898620
hg1998620
hg1898620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv450n100
Supporting Variantsnssv3491048
Samples
Known GenesFCGR2C, 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)nsv1011277
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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