A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101988



Internal ID21272747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:14239074..14241621hg38UCSC Ensembl
Innerchr21:15611395..15613942hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg382548
hg192548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114185
Supporting Variants
Samplessample181
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101988
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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