A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584159



Internal ID16371568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:200119186..200153698hg38UCSC Ensembl
Innerchr2:200983909..201018421hg19UCSC Ensembl
Innerchr2:200692154..200726666hg18UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3834513
hg1934513
hg1834513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151129
SamplesHGDP01163
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584159
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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