A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv16n145



Internal ID22813032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42180936..42184989hg38UCSC Ensembl
chr1:42646607..42650660hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg384054
hg194054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113365, nsv3114893
Samplessample53, sample97
Known GenesFOXJ3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv16n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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