A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002376



Internal ID18744908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:5146106..5235477hg38UCSC Ensembl
Innerchr3:5187791..5277162hg19UCSC Ensembl
Innerchr3:5162791..5252162hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3889372
hg1989372
hg1889372
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591638
Samples
Known GenesARL8B, EDEM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002376
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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