A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101999



Internal ID21273359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19019387..19022769hg38UCSC Ensembl
Innerchr21:20391706..20395088hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg383383
hg193383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116379
Supporting Variants
Samplessample190
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101999
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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