A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117698



Internal ID21300964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:42180936..42184085hg38UCSC Ensembl
Innerchr1:42646607..42649756hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg383150
hg193150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv15n145
Supporting Variantsnssv14090301, nssv14091452
Samplessample28, sample290
Known GenesFOXJ3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117698
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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