A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047352



Internal ID19136571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54953335..55243656hg38UCSC Ensembl
Innerchr11:54720811..55011132hg19UCSC Ensembl
Innerchr11:54477387..54767708hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38290322
hg19290322
hg18290322
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1162n100
Supporting Variantsnssv3519052, nssv3510453, nssv3514122, nssv3503726, nssv3520853, nssv3521505, nssv3513435, nssv3513595, nssv3520630, nssv3505905, nssv3509910, nssv3505492
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047352
Frequency
Sample Size11257
Observed Gain11
Observed Loss1
Observed Complex0
Frequencyn/a


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