A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006417



Internal ID19095634
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 StatusM
Merged Variantsdgv451n100
Supporting Variantsnssv3486923
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)nsv1006417
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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