A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589244



Internal ID16029967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:72450..153276hg38UCSC Ensembl
Innerchr3:114133..194959hg19UCSC Ensembl
Innerchr3:89133..169959hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3880827
hg1980827
hg1880827
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8144n54
Supporting Variantsnssv1152227
SamplesHGDP01090
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589244
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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