A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556040



Internal ID16343449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98786404..98979320hg38UCSC Ensembl
Innerchr11:98657134..98850050hg19UCSC Ensembl
Innerchr11:98162344..98355260hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38192917
hg19192917
hg18192917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv781715
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556040
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