A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591969



Internal ID16379378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:147493190..147581487hg38UCSC Ensembl
Innerchr3:147210977..147299274hg19UCSC Ensembl
Innerchr3:148693667..148781964hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3888298
hg1988298
hg1888298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8635n54
Supporting Variantsnssv976380
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591969
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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