A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591966



Internal ID16379375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:147171868..147242318hg38UCSC Ensembl
Innerchr3:146889655..146960105hg19UCSC Ensembl
Innerchr3:148372345..148442795hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3870451
hg1970451
hg1870451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8634n54
Supporting Variantsnssv976378
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591966
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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