A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517552



Internal ID15098159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133054519..133065493hg38UCSC Ensembl
Innerchr11:132924414..132935388hg19UCSC Ensembl
Innerchr11:132429624..132440598hg18UCSC Ensembl
Innerchr11:132429624..132440598hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3810975
hg1910975
hg1810975
hg1710975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652337, nssv659571, nssv670707, nssv658572, nssv694921, nssv691968, nssv681850, nssv696419, nssv668446, nssv669446, nssv674078, nssv684091, nssv672824
Samples
Known GenesOPCML
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517552
Frequency
Sample Size2026
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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