A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091129



Internal ID21290604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:105070220..105099370hg38UCSC Ensembl
Innerchr11:104940947..104970097hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3829151
hg1929151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116083
Supporting Variants
Samplessample61
Known GenesCARD17
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091129
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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