A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014294



Internal ID18756828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4125592..4274957hg38UCSC Ensembl
Innerchr3:4167276..4316641hg19UCSC Ensembl
Innerchr3:4142276..4291641hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38149366
hg19149366
hg18149366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4652n100
Supporting Variantsnssv3590485
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014294
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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