A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552921



Internal ID15993644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1078904..1225711hg38UCSC Ensembl
Innerchr11:1078980..1246941hg19UCSC Ensembl
Innerchr11:1068980..1203517hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38146808
hg19167962
hg18134538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763959
Samples
Known GenesMUC2, MUC5B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552921
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