A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049814



Internal ID19139033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5768359..5791118hg38UCSC Ensembl
Innerchr11:5789589..5812348hg19UCSC Ensembl
Innerchr11:5746165..5768924hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3822760
hg1922760
hg1822760
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1049n100
Supporting Variantsnssv3514695, nssv3512686, nssv3511799, nssv3520324, nssv3519798, nssv3503647, nssv3708333, nssv3708334, nssv3708332, nssv3503189, nssv3708335, nssv3507507, nssv3516205, nssv3512250, nssv3708336, nssv3520966, nssv3708331, nssv3503888, nssv3504418, nssv3508904, nssv3507335, nssv3518218, nssv3513107, nssv3514459
Samples
Known GenesOR52N1, OR52N5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049814
Frequency
Sample Size11257
Observed Gain1
Observed Loss23
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer