A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581166



Internal ID16021889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:20421643..20460101hg38UCSC Ensembl
Innerchr2:20621404..20659862hg19UCSC Ensembl
Innerchr2:20484885..20523343hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3838459
hg1938459
hg1838459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150409
SamplesHGDP00553
Known GenesRHOB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581166
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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