A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553537



Internal ID15994260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11847002..11854702hg38UCSC Ensembl
Innerchr11:11868549..11876249hg19UCSC Ensembl
Innerchr11:11825125..11832825hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg387701
hg197701
hg187701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768191, nssv768188, nssv768179, nssv768180, nssv768182, nssv768186, nssv768187, nssv768181, nssv768189, nssv768183, nssv768178, nssv768185, nssv768184, nssv768190
Samples
Known GenesUSP47
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553537
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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