A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247366



Internal ID21304018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:59043771..59086292hg38UCSC Ensembl
Outerchr11:59043768..59087546hg38UCSC Ensembl
Innerchr11:58811244..58853765hg19UCSC Ensembl
Outerchr11:58811241..58855019hg19UCSC Ensembl
Innerchr11:58567820..58610341hg18UCSC Ensembl
Outerchr11:58567817..58611595hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3843779
hg1943779
hg1843779
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169836
Supporting Variants
SamplesNGO_1
Known GenesLOC283194
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247366
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