A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556579



Internal ID15997302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131681009..131681637hg38UCSC Ensembl
Innerchr11:131550903..131551531hg19UCSC Ensembl
Innerchr11:131056113..131056741hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38629
hg19629
hg18629
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv785120, nssv785121, nssv785119
Samples
Known GenesNTM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556579
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer