A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117808



Internal ID21301074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:42883861..42893559hg38UCSC Ensembl
Innerchr1:43349532..43359230hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg389699
hg199699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105940
Samplessample80
Known GenesLOC339539
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117808
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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