A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv771052



Internal ID16065008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33030935..33033097hg38UCSC Ensembl
Innerchr11:33052481..33054643hg19UCSC Ensembl
Innerchr11:33009057..33011219hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382163
hg192163
hg182163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553993
Supporting Variants
Samples
Known GenesDEPDC7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv771052
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