A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv763592



Internal ID15710862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1073378..1081357hg38UCSC Ensembl
Innerchr11:1073378..1079511hg19UCSC Ensembl
Innerchr11:1063378..1069511hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg387980
hg196134
hg186134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552891
Supporting Variants
Samples
Known GenesMUC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv763592
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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