A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553124



Internal ID16340533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3220993..3222443hg38UCSC Ensembl
Innerchr11:3242223..3243673hg19UCSC Ensembl
Innerchr11:3198799..3200249hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381451
hg191451
hg181451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764554, nssv764556, nssv764553, nssv764551, nssv764552, nssv764555
Samples
Known GenesMRGPRG-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553124
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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