A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115034



Internal ID21298300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41221573..41243779hg38UCSC Ensembl
Innerchr5:41221675..41243881hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3822207
hg1922207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108931
Samplessample193
Known GenesC6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115034
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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