A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590364



Internal ID16377773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:57426900..57471713hg38UCSC Ensembl
Innerchr3:57412627..57457440hg19UCSC Ensembl
Innerchr3:57387667..57432480hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3844814
hg1944814
hg1844814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963363, nssv1151893
SamplesHGDP00828
Known GenesDNAH12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590364
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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