A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117554



Internal ID21300820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:81036558..81066956hg38UCSC Ensembl
Innerchr4:81957712..81988110hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3830399
hg1930399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107198
Samplessample18
Known GenesBMP3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117554
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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