A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049068



Internal ID19138287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54953335..55167766hg38UCSC Ensembl
Innerchr11:54720811..54935242hg19UCSC Ensembl
Innerchr11:54477387..54691818hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38214432
hg19214432
hg18214432
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1160n100
Supporting Variantsnssv3519863
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)nsv1049068
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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