A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593960



Internal ID18545555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65842708..65916742hg38UCSC Ensembl
Innerchr3:65828383..65902417hg19UCSC Ensembl
Innerchr3:65803423..65877457hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3874035
hg1974035
hg1874035
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000854
Supporting Variants
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)nssv3593960
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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