A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555234



Internal ID16342643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66944839..66945581hg38UCSC Ensembl
Innerchr11:66712310..66713052hg19UCSC Ensembl
Innerchr11:66468886..66469628hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38743
hg19743
hg18743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1971n54
Supporting Variantsnssv778541
Samples
Known GenesPC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555234
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