A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591923



Internal ID16379332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:144057254..144143508hg38UCSC Ensembl
Innerchr3:143776096..143862350hg19UCSC Ensembl
Innerchr3:145258786..145345040hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3886255
hg1986255
hg1886255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8627n54
Supporting Variantsnssv975222
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591923
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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