A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552898



Internal ID16340307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1075920..1107170hg38UCSC Ensembl
Innerchr11:1075920..1101078hg19UCSC Ensembl
Innerchr11:1065920..1091078hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3831251
hg1925159
hg1825159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763601
Samples
Known GenesMUC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552898
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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