A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv770390



Internal ID16064346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:29584719..29689544hg38UCSC Ensembl
Innerchr11:29606266..29711091hg19UCSC Ensembl
Innerchr11:29562842..29667667hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38104826
hg19104826
hg18104826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553943
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv770390
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