A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170129



Internal ID21314190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1237573..1292591hg38UCSC Ensembl
Outerchr11:1236229..1301375hg38UCSC Ensembl
Innerchr11:1258803..1313821hg19UCSC Ensembl
Outerchr11:1257459..1322605hg19UCSC Ensembl
Innerchr11:1215379..1270397hg18UCSC Ensembl
Outerchr11:1214035..1279181hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3865147
hg1965147
hg1865147
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245566
SamplesNGO_23
Known GenesMIR6744, MUC5B, TOLLIP
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170129
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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