A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014271



Internal ID18756805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161623061..161668066hg38UCSC Ensembl
Innerchr1:161592851..161637856hg19UCSC Ensembl
Innerchr1:159859475..159904480hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3845006
hg1945006
hg1845006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3497519
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)nsv1014271
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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