A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv772789



Internal ID15720059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45652716..45662567hg38UCSC Ensembl
Innerchr11:45674266..45684117hg19UCSC Ensembl
Innerchr11:45630842..45640693hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg389852
hg199852
hg189852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554198
Supporting Variants
Samples
Known GenesCHST1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv772789
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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