A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591641



Internal ID16379050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128708896..128713872hg38UCSC Ensembl
Innerchr3:128427739..128432715hg19UCSC Ensembl
Innerchr3:129910429..129915405hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg384977
hg194977
hg184977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8575n54
Supporting Variantsnssv973057, nssv973059, nssv973056, nssv973058
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591641
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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