A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768246



Internal ID15715516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11854251..11870714hg38UCSC Ensembl
Innerchr11:11875798..11892261hg19UCSC Ensembl
Innerchr11:11832374..11848837hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3816464
hg1916464
hg1816464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553543
Supporting Variants
Samples
Known GenesUSP47
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv768246
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