A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555988



Internal ID16343397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97056213..97138206hg38UCSC Ensembl
Innerchr11:96927213..97009206hg19UCSC Ensembl
Innerchr11:96432423..96514416hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3881994
hg1981994
hg1881994
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv781664
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555988
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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