A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590513



Internal ID16377922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65210448..65232993hg38UCSC Ensembl
Innerchr3:65196123..65218668hg19UCSC Ensembl
Innerchr3:65171163..65193708hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3822546
hg1922546
hg1822546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8356n54
Supporting Variantsnssv964123
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590513
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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