A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102644



Internal ID21287905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:40210228..40217299hg38UCSC Ensembl
Innerchr22:40606232..40613303hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg387072
hg197072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112832
Supporting Variants
Samplessample41
Known GenesTNRC6B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102644
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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