A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519866



Internal ID15100473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131595302..131612260hg38UCSC Ensembl
Innerchr11:131465196..131482154hg19UCSC Ensembl
Innerchr11:130970406..130987364hg18UCSC Ensembl
Innerchr11:130970406..130987364hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3816959
hg1916959
hg1816959
hg1716959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697092
Samples
Known GenesNTM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519866
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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