A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011951



Internal ID18754487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161533092..161668711hg38UCSC Ensembl
Innerchr1:161502882..161638501hg19UCSC Ensembl
Innerchr1:159769506..159905125hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38135620
hg19135620
hg18135620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv447n100
Supporting Variantsnssv3495534
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)nsv1011951
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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