A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516941



Internal ID15444234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80261501..80279256hg38UCSC Ensembl
Innerchr11:79972545..79990300hg19UCSC Ensembl
Innerchr11:79650193..79667948hg18UCSC Ensembl
Innerchr11:79650193..79667948hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3817756
hg1917756
hg1817756
hg1717756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv678722, nssv664449, nssv658816, nssv679639, nssv656538, nssv657155, nssv699789, nssv685687, nssv688218, nssv653852, nssv669959, nssv682740, nssv665356, nssv658206, nssv677521, nssv691897, nssv672301, nssv689303, nssv653209, nssv654465, nssv673078, nssv653328, nssv670227, nssv693659, nssv656696, nssv654313, nssv687170, nssv654721, nssv687001, nssv653478, nssv660824, nssv655785, nssv654438
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516941
Frequency
Sample Size2026
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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