A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005259



Internal ID18747790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3992384..4073417hg38UCSC Ensembl
Innerchr3:4034068..4115101hg19UCSC Ensembl
Innerchr3:4009068..4090101hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3881034
hg1981034
hg1881034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590404
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)nsv1005259
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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