A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100856



Internal ID21266590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19020759..19023267hg38UCSC Ensembl
Innerchr21:20393078..20395586hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg382509
hg192509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111402
Supporting Variants
Samplessample10
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100856
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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