A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549661



Internal ID15990384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248576215..248631809hg38UCSC Ensembl
Innerchr1:248739516..248795110hg19UCSC Ensembl
Innerchr1:246806139..246861733hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3855595
hg1955595
hg1855595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv913n54
Supporting Variantsnssv739804, nssv739805, nssv739834, nssv739831, nssv739810, nssv739829, nssv739817, nssv739830, nssv739814, nssv739826, nssv739827, nssv739832, nssv739819, nssv739816, nssv739809, nssv739812, nssv739824, nssv739813, nssv739803, nssv739807, nssv739818, nssv739806, nssv739808, nssv739825, nssv739833, nssv739820, nssv739815, nssv739811, nssv739821, nssv739823, nssv739822, nssv739828
Samples
Known GenesOR2T10, OR2T11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549661
Frequency
Sample Size17421
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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