A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517407



Internal ID15098014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133450180..133451072hg38UCSC Ensembl
Innerchr11:133320075..133320967hg19UCSC Ensembl
Innerchr11:132825285..132826177hg18UCSC Ensembl
Innerchr11:132825285..132826177hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38893
hg19893
hg18893
hg17893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv658008, nssv652616, nssv673599, nssv664724, nssv684239, nssv657981, nssv685836, nssv685864, nssv663879, nssv663354, nssv654798, nssv667558, nssv665532, nssv653849, nssv658635, nssv654436, nssv667912, nssv677356, nssv664972, nssv678924, nssv657152, nssv664940, nssv684562, nssv653919, nssv656562, nssv662808, nssv652593, nssv660772, nssv693091, nssv658708, nssv693894, nssv691099, nssv668841, nssv653206, nssv670038, nssv653993, nssv654719, nssv661870, nssv663333, nssv666548, nssv665986
Samples
Known GenesOPCML
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517407
Frequency
Sample Size2026
Observed Gain0
Observed Loss41
Observed Complex0
Frequencyn/a


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