A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555193



Internal ID16342602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64339671..64353102hg38UCSC Ensembl
Innerchr11:64107143..64120574hg19UCSC Ensembl
Innerchr11:63863719..63877150hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3813432
hg1913432
hg1813432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv777157
Samples
Known GenesCCDC88B, MIR7155
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555193
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