A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764465



Internal ID16058421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1752247..1782412hg38UCSC Ensembl
Innerchr11:1773477..1803642hg19UCSC Ensembl
Innerchr11:1730053..1760218hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3830166
hg1930166
hg1830166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553048
Supporting Variants
Samples
Known GenesCTSD, MOB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764465
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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