A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556521



Internal ID15997244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125208300..125210799hg38UCSC Ensembl
Innerchr11:125078196..125080695hg19UCSC Ensembl
Innerchr11:124583406..124585905hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382500
hg192500
hg182500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784703
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556521
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