A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549619



Internal ID15990342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:247991705..248047570hg38UCSC Ensembl
Innerchr1:248155007..248210872hg19UCSC Ensembl
Innerchr1:246221630..246277495hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3855866
hg1955866
hg1855866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv903n54
Supporting Variantsnssv739727
Samples
Known GenesOR2L13, OR2L2, OR2L5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549619
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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