A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115233



Internal ID21298499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:10287784..10294225hg38UCSC Ensembl
Innerchr19:10398460..10404901hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg386442
hg196442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099614
Samplessample116
Known GenesICAM4, ICAM5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115233
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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