A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522568



Internal ID15103175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93497971..93506741hg38UCSC Ensembl
Innerchr11:93231137..93239907hg19UCSC Ensembl
Innerchr11:92870785..92879555hg18UCSC Ensembl
Innerchr11:92870785..92879555hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg388771
hg198771
hg188771
hg178771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv79n21
Supporting Variantsnssv705952
Samples
Known GenesSMCO4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522568
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