A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012099



Internal ID18754635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65899988..65979750hg38UCSC Ensembl
Innerchr3:65885663..65965425hg19UCSC Ensembl
Innerchr3:65860703..65940465hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3879763
hg1979763
hg1879763
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593961
Samples
Known GenesMAGI1, MAGI1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012099
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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