A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590917



Internal ID16378326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:87061524..87187391hg38UCSC Ensembl
Innerchr3:87110674..87236541hg19UCSC Ensembl
Innerchr3:87193364..87319231hg18UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg38125868
hg19125868
hg18125868
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152496
SamplesHGDP00721
Known GenesLINC00506
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590917
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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