A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2852446



Internal ID15338276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161539698..161676786hg38UCSC Ensembl
Innerchr1:161509488..161646576hg19UCSC Ensembl
Innerchr1:159776112..159913200hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38137089
hg19137089
hg18137089
Variant TypeCNV gain
Copy Number5
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514915
Supporting Variants
SamplesNA18608
Known GenesFCGR2B, FCGR2C, FCGR3A, FCGR3B, HSPA7
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2852446
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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