A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590150



Internal ID16030873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:42984494..43021914hg38UCSC Ensembl
Innerchr3:43025986..43063406hg19UCSC Ensembl
Innerchr3:43000990..43038410hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3837421
hg1937421
hg1837421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151767
SamplesHGDP00514
Known GenesFAM198A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590150
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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