A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593056



Internal ID16380465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195844153..195929860hg38UCSC Ensembl
Innerchr3:195571024..195656731hg19UCSC Ensembl
Innerchr3:197055421..197141128hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3885708
hg1985708
hg1885708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv986852
Samples
Known GenesMIR6829, TNK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593056
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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