A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517199



Internal ID15097806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130155050..130206439hg38UCSC Ensembl
Innerchr11:130024945..130076334hg19UCSC Ensembl
Innerchr11:129530155..129581544hg18UCSC Ensembl
Innerchr11:129530155..129581544hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3851390
hg1951390
hg1851390
hg1751390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700230, nssv696967, nssv669701, nssv671514, nssv667420, nssv653992, nssv677807, nssv685085, nssv688570, nssv672237, nssv692888, nssv665624, nssv670950, nssv684796
Samples
Known GenesST14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517199
Frequency
Sample Size2026
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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