A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555208



Internal ID15995931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64877647..65003707hg38UCSC Ensembl
Innerchr11:64645119..64771179hg19UCSC Ensembl
Innerchr11:64401695..64527755hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38126061
hg19126061
hg18126061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv777172
Samples
Known GenesATG2A, BATF2, C11orf85, EHD1, GPHA2, MIR192, MIR194-2, MIR6749, MIR6750, PPP2R5B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555208
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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