A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102553



Internal ID21287396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41851325..41857397hg38UCSC Ensembl
Innerchr21:43271434..43277506hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg386073
hg196073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111635
Supporting Variants
Samplessample400
Known GenesPRDM15
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102553
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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