A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093145



Internal ID21282152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:46570842..46580346hg38UCSC Ensembl
Innerchr11:46592392..46601896hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg389505
hg199505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111147
Supporting Variants
Samplessample322
Known GenesAMBRA1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093145
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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