A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116664



Internal ID21299930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:21750805..21752135hg38UCSC Ensembl
Innerchr21:23123125..23124455hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381331
hg191331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv702n145
Supporting Variantsnssv14102008, nssv14101984, nssv14101992, nssv14101965
Samplessample184, sample159, sample173, sample197
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116664
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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