A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113046



Internal ID21296312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45277715..45321666hg38UCSC Ensembl
Innerchr21:46697630..46741581hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3843952
hg1943952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102088
Samplessample291
Known GenesLOC642852, POFUT2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113046
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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