A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007959



Internal ID18750490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65724045..65902469hg38UCSC Ensembl
Innerchr3:65709720..65888144hg19UCSC Ensembl
Innerchr3:65684760..65863184hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38178425
hg19178425
hg18178425
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4769n100
Supporting Variantsnssv3593958
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)nsv1007959
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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