A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100946



Internal ID21293123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:25372689..25374005hg38UCSC Ensembl
Innerchr21:26745003..26746319hg19UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg381317
hg191317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117827
Supporting Variants
Samplessample96
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100946
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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