A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3487026



Internal ID19074667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161623061..161667183hg38UCSC Ensembl
Innerchr1:161592851..161636973hg19UCSC Ensembl
Innerchr1:159859475..159903597hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3844123
hg1944123
hg1844123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997933
Supporting Variants
Samples
Known GenesFCGR2B, FCGR3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3487026
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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