A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778622



Internal ID16072578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:68460324..68460995hg38UCSC Ensembl
Innerchr11:68227792..68228463hg19UCSC Ensembl
Innerchr11:67984368..67985039hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38672
hg19672
hg18672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555289
Supporting Variants
Samples
Known GenesPPP6R3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778622
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