A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv451n100



Internal ID22786538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161532055..161678819hg38UCSC Ensembl
chr1:161501845..161648609hg19UCSC Ensembl
chr1:159768469..159915233hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38146765
hg19146765
hg18146765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006417, nsv1014122
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)dgv451n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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