A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555102



Internal ID16342511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:57376679..57378467hg38UCSC Ensembl
Innerchr11:57144152..57145940hg19UCSC Ensembl
Innerchr11:56900728..56902516hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381789
hg191789
hg181789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv776873
Samples
Known GenesPRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555102
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