A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv964210



Internal ID15911480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65811865..65933794hg38UCSC Ensembl
Innerchr3:65797540..65919469hg19UCSC Ensembl
Innerchr3:65772580..65894509hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38121930
hg19121930
hg18121930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590548
Supporting Variants
Samples
Known GenesMAGI1, MAGI1-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv964210
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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