A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590379



Internal ID16377788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:58628289..58656725hg38UCSC Ensembl
Innerchr3:58614016..58642452hg19UCSC Ensembl
Innerchr3:58589056..58617492hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3828437
hg1928437
hg1828437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151894
SamplesHGDP00774
Known GenesFAM3D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590379
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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