A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3492009



Internal ID19079650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161548149..161668711hg38UCSC Ensembl
Innerchr1:161517939..161638501hg19UCSC Ensembl
Innerchr1:159784563..159905125hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38120563
hg19120563
hg18120563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009316
Supporting Variants
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)nssv3492009
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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