A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3486923



Internal ID19074564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161543969..161678819hg38UCSC Ensembl
Innerchr1:161513759..161648609hg19UCSC Ensembl
Innerchr1:159780383..159915233hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38134851
hg19134851
hg18134851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006417
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)nssv3486923
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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