A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009265



Internal ID18751796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3935472..4210583hg38UCSC Ensembl
Innerchr3:3977156..4252267hg19UCSC Ensembl
Innerchr3:3952156..4227267hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38275112
hg19275112
hg18275112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4641n100
Supporting Variantsnssv3590402
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)nsv1009265
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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