A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552891



Internal ID15993614
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 StatusM
Merged Variants
Supporting Variantsnssv763592, nssv763593
Samples
Known GenesMUC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552891
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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